Inhibitors of aggrecanase and matrix metalloproteinases for the treatment of arthritis

ABSTRACT

This invention relates to molecules which inhibit metalloproteinases, including aggrecanase, and the production of tumor necrosis factor (TNF). In particular, the compounds are inhibitors of metalloproteinases involved in tissue degradation and inhibitors of the release of tumor necrosis factor. The present invention also relates to pharmaceutical compositions comprising such compounds and to methods of using these compounds for the treatment of inflammatory diseases.

This application claims the benefit of U.S. Provisional Application No. 60/055,944 filed Aug. 18, 1997 and U.S. Provisional Application No. 60/068,335 filed on Dec. 19, 1997.

FIELD OF THE INVENTION

The present invention relates to novel molecules which inhibit metalloproteinases, including aggrecanase, and the production of tumor necrosis factor (TNF), pharmaceutical preparations containing them and to their use as pharmaceutical agents. In particular the compounds are inhibitors of metalloproteinases involved in tissue degradation and inhibitors of the release of tumor necrosis factor.

BACKGROUND OF THE INVENTION

There is now a body of evidence that metalloproteinases (MP) are important in the uncontrolled breakdown of connective tissue, including proteoglycan and collagen, leading to resorption of the extracellular matrix. This is a feature of many pathological conditions, such as rheumatoid and osteoarthritis, corneal, epidermal or gastric ulceration; tumor metastasis or invasion; periodontal disease and bone disease. Normally these catabolic enzymes are tightly regulated at the level of their synthesis as well as at their level of extracellular activity through the action of specific inhibitors, such as alpha-2-macroglobulins and TIMP (tissue inhibitor of metalloproteinase), which form inactive complexes with the MP's.

Osteo- and Rheumatoid Arthritis (OA and RA respectively) are destructive diseases of articular cartilage characterized by localized erosion of the cartilage surface. Findings have shown that articular cartilage from the femoral heads of patients with OA, for example, had a reduced incorporation of radiolabeled sulfate over controls, suggesting that there must be an enhanced rate of cartilage degradation in OA (Mankin et al. J. Bone Joint Surg. 52A, 1970, 424-434). There are four classes of protein degradative enzymes in mammalian cells: serine, cysteine, aspartic and metalloproteinases. The available evidence supports that it is the metalloproteinases which are responsible for the degradation of the extracellular matrix of articullar cartilage in OA and RA. Increased activities of collagenases and stromelysin have been found in OA cartilage and the activity correlates with severity of the lesion (Mankin et al. Arthritis Rheum. 21, 1978, 761-766, Woessner et al. Arthritis Rheum. 26, 1983, 63-68 and Ibid. 27, 1984, 305-312). In addition, aggrecanase (a newly identified metalloproteinase enzymatic activity) has been identified that provides the specific cleavage product of proteoglycan, found in RA and OA patients (Lohmander L. S. et al. Arthritis Rheum. 36, 1993, 1214-22).

Therefore metalloproteinases (MP) have been implicated as the key enzymes in the destruction of mammalian cartilage and bone. It can be expected that the pathogenesis of such diseases can be modified in a beneficial manner by the administration of MP inhibitors, and many compounds have been suggested for this purpose (see Wahl et al. Ann. Rep. Med. Chem. 25, 175-184, AP, San Diego, 1990).

This invention describes novel molecules that inhibit aggrecanase and other metalloproteinases. These novel molecules are provided as cartilage protecting therapeutics. The inhibition of aggrecanase and other metalloproteinases by these novel molecules prevent the degradation of cartilage by these enzymes, thereby alleviating the pathological conditions of osteo- and rheumatoid arthritis.

Tumor necrosis factor (TNF) is a cell associated cytokine that is processed from a 26 kD precursor form to a 17 kD active form. TNF has been shown to be a primary mediator in humans and in animals, of inflammation, fever, and acute phase responses, similar to those observed during acute infection and shock. Excess TNF has been shown to be lethal. There is now considerable evidence that blocking the effects of TNF with specific antibodies can be beneficial in a variety of circumstances including autoimmune diseases such as rheumatoid arthritis (Feldman et al, Lancet, 1994, 344, 1105) and non-insulin dependent diabetes melitus. (Lohmander L.S. et al. Arthritis Rheum. 36, 1993, 1214-22) and Crohn's disease (Macdonald T. et al. Clin. Exp. Immunol. 81, 1990, 301).

Compounds which inhibit the production of TNF are therefore of therapeutic importance for the treatment of inflammatory disorders. Recently it has been shown that a matrix metalloproteinase or family of metalloproteinases, hereafter known as TNF-convertases (TNF-C), as well as other MP's are capable of cleaving TNF from its inactive to active form (Gearing et al Nature, 1994, 370, 555). This invention describes novel molecules that inhibit this conversion and hence the secretion of active TNF-α from cells. These novel molecules provide a means of mechanism based therapeutic intervention for diseases including but not restricted to septic shock, haemodynamic shock, sepsis syndrome, post ischaemic reperfusion injury, malaria, Crohn's disease, inflammatory bowel diseases, mycobacterial infection, meningitis, psoriasis, congestive heart failure, fibrotic diseases, cachexia, graft rejection, cancer, diseases involving angiogenesis, autoimmune diseases, skin inflammatory diseases, rheumatoid arthritis, multiple sclerosis, radiation damage, hyperoxic alveolar injury, HIV and non-insulin dependent diabetes melitus.

Since excessive TNF production has been noted in several disease conditions also characterized by MMP-mediated tissue degradation, compounds which inhibit both MMPs and TNF production may also have a particular advantage in diseases where both mechanisms are involved.

There are several patents which disclose hydroxamate and carboxylate based MMP inhibitors.

PCT International Publication No. WO 92/213260 describes N-carboxyalkylpeptidyl compounds of general formula:

wherein AA is an amino acid, as inhibitors of matrix metallproteinase mediated diseases.

PCT International Publication No. WO 90/05716 discloses hydroxamic acid based collagenase inhibitors having the general formula:

PCT International Publication No. WO 92/13831 describes related hydroxamic acids having collagenase inhibiting activity with the general formula:

PCT International Publication No. WO 94/02446 discloses metalloproteinase inhibitors which are natural amino acid derivatives of general formula:

WO95/09841 describes compounds that are hydroxamic acid derivatives and are inhibitors of cytokine production.

European Patent Application Publication No. 574,758 A1, discloses hydroxamic acid derivatives as collagenase inhibitors having the general formula:

GB 2 268 934 A and WO 94/24140 claim hydroxamate inhibitors of MMPs as inhibitors of TNF production.

The compounds of the current invention act as inhibitors of MPs, in particular aggrecanase and TNF-C, thereby preventing cartilage loss and destruction and inflammatory disorders involving TNF. The hydroxamic and carboxylic acids and derivatives contain a cyclic peptide mimic attached to a succinate peptide mimic, and thus the inhibitors are non-peptide in nature. A selection of these molecules are water soluble and are orally bioavailable.

SUMMARY OF THE INVENTION

This invention provides novel hydroxamic acids and carboxylic acids and derivatives thereof of formula (I) (described below) which are useful as inhibitors of metalloproteinases, such as aggrecanase and TNF-C. The present invention also includes pharmaceutical compositions comprising such compounds of formula (I) and methods of using such compounds for the treatment of arthritis and other inflammatory disorders as described previously, in a patient.

Also included in the present invention are pharmaceutical kits comprising one or more containers containing pharmaceutical dosage units comprising a compound of formula (I), for the treatment of arthritis and other inflammatory disorders as described previously.

The present invention also includes methods of inhibiting metalloproteinases, such as aggrecanase and TNF-C, and for the treatment of arthritis by administering a compound of formula (I) in combination with one or more second therapeutic agents selected from other inhibitors of metalloproteinases, such as aggrecanase and TNF-C and/or therapeutic agents for the treatment of arthritis and inflammation.

DETAILED DESCRIPTION OF THE INVENTION

This invention provides novel hydroxamic acids and carboxylic acids and derivatives thereof of formula (I) (described below) which are useful as inhibitors of metalloproteinases, such as aggrecanase and TNF-C. The present invention also includes pharmaceutical compositions comprising such compounds of formula (I) and methods of using such compounds for the treatment of arthritis and other inflammatory disorders as described previously, in a patient.

Also included in the present invention are pharmaceutical kits comprising one or more containers containing pharmaceutical dosage units comprising a compound of formula (I), for the treatment of arthritis and other inflammatory disorders as described previously.

The present invention also includes methods of inhibiting metalloproteinases, such as aggrecanase and tumor necrosis factor alpha, and for the treatment of arthritis by administering a compound of formula (I) in combination with one or more second therapeutic agents selected from other inhibitors of metalloproteinases, such as aggrecanase and tumor necrosis factor alpha and/or therapeutic agents for the treatment of arthritis and inflammation.

DEFINITIONS

The compounds herein described may have asymmetric centers. Compounds of the present invention containing an asymmetrically substituted atom may be isolated in optically active or racemic forms. It is well known in the art how to prepare optically active forms, such as by resolution of racemic forms or by synthesis from optically active starting materials. Many geometric isomers of olefins, C═N double bonds, and the like can also be present in the compounds described herein, and all such stable isomers are contemplated in the present invention. Cis and trans geometric isomers of the compounds of the present invention are described and may be isolated as a mixture of isomers or as separated isomeric forms. All chiral, diastereomeric, racemic forms and all geometric isomeric forms of a structure are intended, unless the specific stereochemistry or isomeric form is specifically indicated.

The term “substituted,” as used herein, means that any one or more hydrogens on the designated atom is replaced with a selection from the indicated group, provided that the designated atom's normal valency is not exceeded, and that the substitution results in a stable compound. When a substitent is keto (i.e., ═O), then 2 hydrogens on the atom are replaced.

When any variable (e.g., R^(b)) occurs more than one time in any constituent or formula for a compound, its definition at each occurrence is independent of its definition at every other occurrence. Thus, for example, if a group is shown to be substituted with 0-2 R⁶, then said group may optionally be substituted with up to two R⁶ groups and R⁶ at each occurrence is selected independently from the definition of R⁶. Also, combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.

When a bond to a substituent is shown to cross a bond connecting two atoms in a ring, then such substituent may be bonded to any atom on the ring. When a substituent is listed without indicating the atom via which such substituent is bonded to the rest of the compound of a given formula, then such substituent may be bonded via any atom in such substituent. Combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.

As used herein, “H” is intended to include substitutions with deuterium or tritium. Where “H” is not indicated but is part of a bond then substitutions with deuterium or tritium are also intentded.

As used herein, “C₁₋₁₀ alkyl” or “C₁₋₁₀ alkylene” is intended to include both branched and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms, examples of which include, but are not limited to, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, t-butyl, pentyl, and hexyl;

“Alkenyl” or “alkenylene” is intended to include hydrocarbon chains of either a straight or branched configuration and one or more unsaturated carbon-carbon bonds which may occur in any stable point along the chain, such as ethenyl, propenyl, and the like.

“Alkynyl” or “alkynylene” is intended to include hydrocarbon chains of either a straight or branched configuration and one or more carbon-carbon triple bonds which may occur in any stable point along the chain, such as ethynyl, propynyl, and the like.

As used herein, “aryl” or “aromatic residue” is intended to include phenyl or naphthyl as well as commonly referred to “heterocycle” or “heteroaryl” or “heterocyclic” compounds.

As used herein the term “alkylaryl” represents an aryl group attached through an alkyl bridge.

“Halo” or “halogen” as used herein refers to fluoro, chloro, bromo, and iodo; and “counterion” is used to represent a small, negatively charged species such as chloride, bromide, hydroxide, acetate, sulfate, and the like.

As used herein, “carbocycle” or “carbocyclic residue” is intended to mean any stable 3- to 7-membered monocyclic or bicyclic or 7- to 13-membered bicyclic or tricyclic, any of which may be saturated, partially unsaturated, or aromatic. Examples of such carbocycles include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, adamantyl, cyclooctyl, [3.3.0]bicyclooctane, [4.3.0]bicyclononane, [4.4.0]bicyclodecane (decalin), [2.2.2]bicyclooctane, fluorenyl, phenyl, naphthyl, indanyl, adamantyl, or tetrahydronaphthyl (tetralin).

As used herein, the term “heterocycle”,or “heterocyclic system” is intended to mean a stable 5- to 7-membered monocyclic or bicyclic or 7- to 14-membered bicyclic heterocyclic ring which is saturated partially unsaturated or unsaturated (aromatic), and which consists of carbon atoms and from 1 to 4 heteroatoms independently selected from the group consisting of N, O and S and including any bicyclic group in which any of the above-defined heterocyclic rings is fused to a benzene ring. The nitrogen and sulfur heteroatoms may optionally be oxidized. The heterocyclic ring may be attached to its pendant group at any heteroatom or carbon atom which results in a stable structure. The heterocyclic rings described herein may be substituted on carbon or on a nitrogen atom if the resulting compound is stable. If specifically noted, a nitrogen in the heterocycle may optionally be quaternized. It is preferred that when the total number of S and O atoms in the heterocycle exceeds 1, then these heteroatoms are not adjacent to one another. It is preferred that the total number of S and O atoms in the heterocycle is not more than 1.

As used herein, the term “aromatic heterocyclic system” is intended to mean a stable 5- to 7-membered monocyclic or bicyclic or 7- to 14-membered bicyclic heterocyclic aromatic ring which consists of carbon atoms and from 1 to 4 heterotams independently selected from the group consisting of N, O and S. It is preferred that the total number of S and O atoms in the aromatic heterocycle is not more than 1.

Examples of heterocycles include, but are not limited to, 1H-indazole, 2-pyrrolidonyl, 2H,6H-1,5,2-dithiazinyl, 2H-pyrrolyl, 3H-indolyl, 4-piperidonyl, 4aH-carbazole, 4H-quinolizinyl, 6H-1,2,5-thiadiazinyl, acridinyl, azocinyl, benzimidazolyl, benzofuranyl, benzothiofuranyl, benzothiophenyl, benzoxazolyl, benzthiazolyl, benztriazolyl, benztetrazolyl, benzisoxazolyl, benzisothiazolyl, benzimidazalonyl, carbazolyl, 4aH-carbazolyl, b-carbolinyl, chromanyl, chromenyl, cinnolinyl, decahydroquinolinyl, 2H,6H-1,5,2-dithiazinyl, dihydrofuro[2,3-b]tetrahydrofuran, furanyl, furazanyl, imidazolidinyl, imidazolinyl, imidazolyl, 1H-indazolyl, indolenyl, indolinyl, indolizinyl, indolyl, isobenzofuranyl, isochromanyl, isoindazolyl, isoindolinyl, isoindolyl, isoquinolinyl, isothiazolyl, isoxazolyl, morpholinyl, naphthyridinyl, octahydroisoquinolinyl, oxadiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, oxazolidinyl, oxazolyl, oxazolidinylperimidinyl, phenanthridinyl, phenanthrolinyl, phenarsazinyl, phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, phthalazinyl, piperazinyl, piperidinyl, pteridinyl, piperidonyl, 4-piperidonyl, pteridinyl, purinyl, pyranyl, pyrazinyl, pyrazolidinyl, pyrazolinyl, pyrazolyl, pyridazinyl, pyridooxazole, pyridoimidazole, pyridothiazole, pyridinyl, pyridyl, pyrimidinyl, pyrrolidinyl, pyrrolinyl, pyrrolyl, quinazolinyl, quinolinyl, 4H-quinolizinyl, quinoxalinyl, quinuclidinyl, carbolinyl, tetrahydrofuranyl, tetrahydroisoquinolinyl, tetrahydroquinolinyl, 6H-1,2,5-thiadiazinyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, thianthrenyl, thiazolyl, thienyl, thienothiazolyl, thienooxazolyl, thienoimidazolyl, thiophenyl, triazinyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl, xanthenyl. Preferred heterocycles include, but are not limited to, pyridinyl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, indolyl, benzimidazolyl, 1H-indazolyl, oxazolidinyl, benzotriazolyl, benzisoxazolyl, oxindolyl, benzoxazolinyl, or isatinoyl. Also included are fused ring and spiro compounds containing, for example, the above heterocycles.

The term “amino acid” as used herein means an organic compound containing both a basic amino group and an acidic carboxyl group. Included within this term are natural amino acids (e.g., L-amino acids), modified and unusual amino acids (e.g., D-amino acids), as well as amino acids which are known to occur biologically in free or combined form but usually do not occur in proteins. Included within this term are modified and unusual amino acids, such as those disclosed in, for example, Roberts and Vellaccio (1983) The Peptides, 5: 342-429, the teaching of which is hereby incorporated by reference. Natural protein occurring amino acids include, but are not limited to, alanine, arginine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, serine, threonine, tyrosine, tyrosine, tryptophan, proline, and valine. Natural non-protein amino acids include, but are not limited to arginosuccinic acid, citrulline, cysteine sulfinic acid, 3,4-dihydroxyphenylalanine, homocysteine, homoserine, ornithine, 3-monoiodotyrosine, 3,5-diiodotryosine, 3,5,5′-triiodothyronine, and 3,3′,5,5′-tetraiodothyronine. Modified or unusual amino acids which can be used to practice the invention include, but are not limited to, D-amino acids, hydroxylysine, 4-hydroxyproline, an N-Cbz-protected amino acid, 2,4-diaminobutyric acid, homoarginine, norleucine, N-methylaminobutyric acid, naphthylalanine, phenylglycine, β-phenylproline, tert-leucine, 4-aminocyclohexylalanine, N-methyl-norleucine, 3,4-dehydroproline, N,N-dimethylaminoglycine, N-methylaminoglycine, 4-aminopiperidine-4-carboxylic acid, 6-aminocaproic acid, trans-4-(aminomethyl)-cyclohexanecarboxylic acid, 2-, 3-, and 4-(aminomethyl)-benzoic acid, 1-aminocyclopentanecarboxylic acid, 1-aminocyclopropanecarboxylic acid, and 2-benzyl-5-aminopentanoic acid.

The phrase “pharmaceutically acceptable” is employed herein to refer to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.

As used herein, “pharmaceutically acceptable salts” refer to derivatives of the disclosed compounds wherein the parent compound is modified by making acid or base salts thereof. Examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of basic residues such as amines; alkali or organic salts of acidic residues such as carboxylic acids; and the like. The pharmaceutically acceptable salts include the conventional non-toxic salts or the quaternary ammonium salts of the parent compound formed, for example, from non-toxic inorganic or organic acids. For example, such conventional non-toxic salts include those derived from inorganic acids such as hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric, nitric and the like; and the salts prepared from organic acids such as acetic, propionic, succinic, glycolic, stearic, lactic, malic, tartaric, citric, ascorbic, pamoic, maleic, hydroxymaleic, phenylacetic, glutamic, benzoic, salicylic, sulfanilic, 2-acetoxybenzoic, fumaric, toluenesulfonic, methanesulfonic, ethane disulfonic, oxalic, isethionic, and the like.

The pharmaceutically acceptable salts of the present invention can be synthesized from the parent. compound which contains a basic or acidic moiety by conventional chemical methods. Generally, such salts can be prepared by reacting the free acid or base forms of these compounds with a stoichiometric amount of the appropriate base or acid in water or in an organic solvent, or in a mixture of the two; generally, nonaqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile are preferred. Lists of suitable salts are found in Remington's Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton, Pa., 1985, p. 1418, the disclosure of which is hereby incorporated by reference.

“Prodrugs” and “prodrug derivatives” are intended to include any covalently bonded carriers which release the active parent drug according to formula (I) in vivo when such prodrug is administered to a mammalian subject. Prodrugs of a compound of formula (I) are prepared by modifying functional groups present in the compound in such a way that the modifications are cleaved, either in routine manipulation or in vivo, to the parent compound. Prodrugs include compounds of formula (I) wherein a hydroxy, amino, or sulfhydryl group is bonded to any group that, when the prodrug or compound of formula (I) is administered to a mammalian subject, cleaves to form a free hydroxyl, free amino, or free sulfhydryl group, respectively. Examples of prodrugs include, but are not limited to, acetate, formate and benzoate derivatives of alcohol and amine functional groups in the compounds of formula (I), and the like.

“Stable compound” and “stable structure” are meant to indicate a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into an efficacious therapeutic agent.

[1] There is provided by this invention a compound of the formula (I):

or a pharmaceutically acceptable salt form or a steroisomer thereof, wherein:

R¹ is selected from:

—CO₂H, —C(O)NHOH, —C(O)NHOR⁷, —SH, —CH₂CO₂R⁷, —COR⁷, —N(OH)COR⁷, —SN₂H₂R⁷, —SONHR⁷, —CH₂CO₂H, —PO(OH)₂, —PO(OH)NHR⁷, —CH₂SH, —C(O)NHOR⁷, —CO₂R⁷, and common prodrug derivatives;

R² is selected from the formula:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R³ is selected from the formula:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R⁴ is selected from:

hydrogen, (C₁-C₅)alkyl, (C₁-C₅)alkyl-aryl,

R⁵ and R⁶ are independently selected from:

 U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R⁷ is selected from: C₁-C₁₀ alkyl, alkylaryl, and common prodrug derivatives

A is selected from:

SO₂, SO, CHOH;

E is (CR⁸R⁹)_(m)—W—(CR⁸R⁹)_(n),

wherein W can be absent or selected from:

CH₂, CO, O, S(O)_(m) and NR¹⁰,

m is 0-2,

n is 0-2;

with the proviso that when W is O, S or NR¹⁰ then m must not be 0;

R⁸ and R⁹ is independently selected from:

H,

C₁-C₈ alkyl substituted with 0-5 R^(b),

C₁-C₈ alkenyl,

C₁-C₈ alkylaryl substituted with 0-5 R^(b),

C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b),

5-14 membered heterocyclic system containing from

1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

amino,

C₁-C₈ alkyl-NR¹⁰

hydroxyl,

R⁸ and R⁹ can also form a ring interrupted by NR¹⁰, O, S(O)m.

R¹⁰ is selected from:

hydrogen,

C₁-C₈ alkyl

C₁-C₈ alkylaryl

J¹, J², J³, J⁴ are independently selected from:

CH, or N.

with no more than two N in the cycle.

[2] The present invention includes compounds of formula (I) wherein:

R¹ is selected from: —CO₂H, —C(O)NHOH, —C(O)NHOR⁷, —SH, —CH₂CO₂R⁷, —COR⁷, —N(OH)COR⁷, —SN₂H₂R⁷, —SONHR⁷, —CH₂CO₂H, —PO(OH)₂, —PO(OH)NHR⁷, —CH₂SH, —C(O)NHOR⁷, —CO₂R⁷, and common prodrug derivatives;

R² is selected from the formula:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

, at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R³ is selected from the formula:

 U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

, at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R⁴ is selected from:

hydrogen,

R⁵ and R⁶ are independently selected from:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R⁷ is selected from: C₁-C₁₀ alkyl, alkylaryl, and common prodrug derivatives

A is selected from:

SO₂, SO, CHOH;

E is (CR⁸R⁹)_(m)—W—(CR⁸R⁹)_(n),

wherein W can be absent or selected from:

CH₂, CO, O, S(O)_(m) and NR¹⁰,

m is 0-2,

n is 0-2;

with the proviso that when w is O, S or NR^(10 then)

m must not be 0;

R⁸ and R⁹ is independently selected from:

H,

C₁-C₈ alkyl substituted with 0-5 R^(b),

C₁-C₈ alkenyl,

C₁-C₈ alkylaryl substituted with 0-5 R^(b),

C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b),

5-14 membered heterocyclic system containing from

1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

amino,

C₁-C₈ alkyl-NR¹⁰

hydroxyl,

R⁸ and R⁹ can also form a ring interrupted by NR¹⁰, O, S(O)m.

R¹⁰ is selected from:

hydrogen,

C₁-C₈ alkyl

C₁-C₈ alkylaryl

J¹, J², J³, J⁴ are independently selected from:

CH, or N.

with no more than two N in the cycle.

[3] The present invention includes preferred compounds of formula (I) wherein:

R¹ is selected from:

—CO₂H, —C(O)NHOH, —C(O)NHOR⁷, —SH, —CH₂CO₂R⁷,

and common prodrug derivatives;

R² is selected from the formula:

 U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R³ is selected from the formula:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R⁴ is selected from:

hydrogen,

R⁵ and R⁶ are independently selected from:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R⁷ is selected from: C₁-C₁₀ alkyl, alkylaryl, and common prodrug derivatives

A is selected from:

SO₂, SO, CHOH;

E is (CR⁸R⁹)_(m)—W—(CR⁸R⁹)_(n),

wherein W can be absent or selected from:

CH₂, CO, O, S(O)_(m) and NR¹⁰,

m is 0-2,

n is 0-2;

with the proviso that when W is O, S or NR¹⁰ then

m must not be 0;

R⁸ and R⁹ is independently selected from:

H,

C₁-C₈ alkyl substituted with 0-5 R^(b),

C₁-C₈ alkenyl,

C₁-C₈ alkylaryl substituted with 0-5 R^(b);

C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b),

5-14 membered heterocyclic system containing from

1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

amino,

C₁-C₈ alkyl-NR¹⁰

hydroxyl,

R⁸ and R⁹ can also form a ring interrupted by NR¹⁰, O, S(O)_(m).

R¹⁰ is selected from:

hydrogen,

C₁-C₈ alkyl

C₁-C₈ alkylaryl

J¹, J², J³, J⁴ are independently selected from:

CH,or N.

with no more than two N in the cycle.

[4] There is provided by this invention preferred compounds of the formula (II):

or a pharmaceutically acceptable salt form or a steroisomer thereof, wherein:

R¹ is selected from:

—CO₂H, —C(O)NHOH, —C(O)NHOR⁷, —SH, —CH₂CO₂R⁷,

and common prodrug derivatives;

R² is selected from the formula:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R³ is selected from the formula:

 U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(OO, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R⁵ is selected from:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R⁷ is selected from: C₁-C₁₀ alkyl, alkylaryl, and common prodrug derivatives

E is (CR⁸R⁹)_(m)—W—(CR⁸R⁹)_(n),

wherein W can be absent or selected from:

CH₂, CO, O, S(O)_(m) and NR¹⁰,

m is 0-2,

n is 0-2;

with the proviso that when W is O, S or NR¹⁰ then

m must not be 0;

R⁸ and R⁹ is independently selected from:

H,

C₁-C₈ alkyl substituted with 0-5 R^(b),

C₁-C₈ alkenyl,

C₁-C₈ alkylaryl substituted with 0-5 R^(b),

C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b),

5-14 membered heterocyclic system containing from

1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

amino,

C₁-C₈ alkyl-NR¹⁰

hydroxyl,

R⁸ and R⁹ can also form a ring interrupted by NR¹⁰, O, S(O)_(m).

R¹⁰ is selected from:

hydrogen,

C₁-C₈ alkyl

C₁-C₈ alkylaryl

J¹, J², J³, J⁴ are independently selected from:

CH, or N.

with no more than two N in the cycle.

[5] Preferred compounds of the present invention include compounds of formula (II) wherein:

R¹ is selected from:

—C(O)NHOH,

and common prodrug derivatives;

R² is selected from the formula:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R³ is selected from the formula:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), C₁, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF_(3, CF) ₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R⁵ is selected from:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R⁷ is selected from: C₁-C₁₀ alkyl, alkylaryl, and common prodrug derivatives

E is (CR⁸R⁹)_(m)—W—(CR⁸R⁹)_(n),

wherein W can be absent or selected from:

CH₂, CO, O, S(O)_(m) and NR¹⁰,

m is 0-2,

n is 0-2;

with the proviso that when W is O, S or NR¹⁰ then

m must not be 0;

R⁸ and R⁹ is independently selected from:

H,

C₁-C₈ alkyl substituted with 0-5 R^(b),

C₁-C₈ alkenyl,

C₁-C₈ alkylaryl substituted with 0-5 R^(b),

C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b),

5-14 membered heterocyclic system containing from

1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

amino,

C₁-C₈ alkyl-NR¹⁰

hydroxyl,

R⁸ and R⁹ can also form a ring interrupted by NR¹⁰, O, S(O)_(m).

R¹⁰ is selected from:

hydrogen,

C₁-C₈ alkyl

C₁-C₈ alkylaryl

J¹, J², J³, J⁴ are independently selected from:

CH, or N.

with no more than two N in the cycle.

[6] More preferred compounds of the present invention are compounds of the formula (III):

or a pharmaceutically acceptable salt form or a steroisomer thereof, wherein:

R¹ is selected from:

—C(O)NHOH

and common prodrug derivatives;

R² is selected from the formula:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R³ is selected from the formula:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H; a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R⁵ is selected from:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a),

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R⁸ and R⁹ is independently selected from:

H,

C₁-C₈ alkyl substituted with 0-5 R^(b),

C₁-C₈ alkenyl,

C₁-C₈ alkylaryl substituted with 0-5 R^(b),

C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b),

5-14 membered heterocyclic system containing from

1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

amino, C₁-C₈ alkyl-NR¹⁰

hydroxyl,

R⁸ and R⁹ can also form a ring interrupted by NR¹⁰, O, S(O)_(m).

R¹⁰ is selected from:

hydrogen,

C₁-C₈ alkyl

C₁-C₈ alkylaryl

J¹, J², J³, J⁴ are independently selected from:

CH, or N.

with no more than two N in the cycle.

[7] The more preferred compounds provided by this invention are compounds of the formula (IV):

or a pharmaceutically acceptable salt form or a steroisomer therof, wherein:

R² is selected from the formula:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, 01-10 alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R³ is selected from the formula:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R⁵ is selected from:

U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a)

wherein:

U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O₎NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

U^(a) is absent or is selected from: H, O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a);

X^(a) is absent or selected from H, C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, C₂₋₁₀ alkynylene;

Y^(a) is absent or selected from H, O, NR^(a), S(O)_(p), and C(O);

Z^(a) is absent or selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c);

R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl or benzyl;

alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃;

R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R⁸ and R⁹ is independently selected from:

H,

C1-C8 alkyl substituted with 0-5 R^(b),

C1-C8 alkenyl,

C1-C8 alkylaryl substituted with 0-5 R^(b),

C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b),

5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b);

amino, C1-C8 alkyl-NR¹⁰

hydroxyl,

R⁸ and R⁹ can also form a ring interrupted by NR¹⁰, O, S(O)m.

R¹⁰ is selected from:

hydrogen,

C1-C8 alkyl

C1-C8 alkylaryl

[8] Most preferred compounds of the present invention include compounds selected from the group consisting of:

N1-(2(R)-hydroxy-1(S)-indanyl)-N4-hydroxy-2(R)-isobutyl-butanediamide;

N1-(2(R)-hydroxy-1(S)-indanyl)-N4-hydroxy-2(R)-isobutyl-3(S)-(5-hydroxycarbonyl)-pentanamide;

N1-(2(R)-hydroxy-1(S)-indanyl)-N4-hydroxy-2(R)-isobutyl-3(S)-methyl-butanediamide;

N1-(2(R)-hydroxy-1(S)-indanyl)-N4-hydroxy-2(R)-isobutyl-3(S)-propyl-butanediamide;

N1-(2(R)-hydroxy-1(S)-indanyl)-N4-hydroxy-2(R)-hexyl-3(S)-propyl-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[4-hydroxy-phenyl)methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[4-methoxy-phenyl)methyl]butanediamide;

N1-[1(S)-indanyl]-N4-hydroxy-2(R)-[4-(hydroxy-phenyl)methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-phenyl-propyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(benzyloxy)-phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[3-(benzyloxy)-phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[4-(fluoro-phenyl)methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3,4-(methylenedioxy-phenyl)methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(methoxy-phenyl)methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3-trifluoromethyl-phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2-tert-butylaminosulfonyl-phenyl)phenyl]methyl]-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2-methoxy-phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-4-methoxy-phenyl)methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[3-(3-thiophene)isoxazoline]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2-chloro-phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2-benzofuran)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2-methyl-phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[3,4-(methylenedioxy-phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2-tetrazole-phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[3-phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[3-methyl-phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[4-(amino-phenyl)methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(benzyloxy-carbonyl)amino]phenyl)methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2-hydroxymethlene)phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3,4,5-trimethoxy-phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2,4-di-methoxy-phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3,5-di-chloro-phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2-trifluoromethyl-phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3-isopropyl-phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2,4-dichloro-phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3-chloro-4-fluoro-phenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(p-toluenesulfonyl-amino)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-phenylmethyl-3(S)-(tert-butyloxy-carbonyl-amino)-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3,4-methylenedioxyphenyl)phenyl]methyl]-3(S)-(tert-butyloxy-carbonyl-amino)-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3-methoxyphenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3-fluorophenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(fluoro-phenyl)methyl]-3(S)-(tert-butyloxy-carbonyl-amino)-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(tert-butyloxy-carbonyl-amino)-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3-nitrophenyl)phenyl]methyl]butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3-(methylsulfonyl-amino)-phenyl)phenyl]methyl]-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(3-trimethylsilyl-propyl)-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2,2-dimethyl-propionamido)-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(ethyloxy-carbonyl-amino)-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(iso-butyloxy-carbonyl-amino)-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(propionamido)-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-methyl-cyclopropane carboxamido-1-yl)-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2,2-dimethylpropyl-amino)-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(methylsulfonyl-amino)-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-amino-butanediamide;

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[4-(methylsulfonylamino)-phenyl)methyl]-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(cyclobutane carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-hydroxymethyl-isobutanamide)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-hydroxyl-cyclopropane carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-phenyl-cyclopropane carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(bezene carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-cyano-cyclopropane carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-phenyl-cyclopentane carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-methyl-cyclohexane carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-indole carboxamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-furan carboxamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-quinoline carboxamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(3,4,5-trimethoxy benzene carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-methyl-3-amino-benzene carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-methyl-6-amino-benzene carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(3-pyridine carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-(2,4-dichloro-phenyl)-cyclopropane carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-(4-chloro-phenyl)-cyclopropane carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(3-methylsulfonyl)-benzene carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-methylsulfonyl-benzene carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(3-cyano-benzene carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(6-quinoline carboxamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-ethyl, 3-methyl-pyrazole 5-carboxamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3-(4-morpholino-benzene carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-chloro-4-methylsulfonyl-benzene carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(4-(imidazol-1-yl)benzene carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-thiophene carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-tert-butyl, 3-methyl-pyrazole 5-carboxamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(4-aminomethyl benzene carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-hydroxyl-isobutanamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(cyclopropane carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(cyclopentane carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-(3-(hydroxy-phenyl)methyl-3(S)-(2cyclopentyl acetamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(cyclohexane carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(4-(4-N-Boc-piperazinyl-1-yl)benzene carboxamido-1-yl)butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(4-(piperazinyl-1-yl)benzene carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-Fluoro-6-chloro-benzene carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-amino-cyclohexane carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-methylthio-acetamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-methoxy-acetamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-allyl-cyclopentane carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-n-propyl-cyclopentane carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-allyl-cyclopropane carboxamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(8-quinoline-sulfonamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(4-nitro-benzene sulfonamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1,4-di-methyl-2-chloro-pyrazole-3-sulfonamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl-3(S)-(1,5-dimethyl-isooxazole-3-sulfonamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-methyl-imidazole 3-sulfonamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(benzene sulfonamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1,4-dimethyl pyrazole 3-sulfonamido)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-methylsulfonyl benzene sulfonamido-1-yl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(cyclohexylamino)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(iso-propylamino)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[4(2-trifluoromethylphenyl)-phenylmethyl]-3(S)-(2,2-dimethylpropyl-amino)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(cyclopentylamino)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(cyclopropylmethyl)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(benzylamino)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-furanmethylamino)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-4-methylphenyl)methyl]-3(S)-(3-cyanophenylmethylamino)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2,2-dimethylpropyl-amino)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-pentylamino)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(bis-cyclopropylmethyamino)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-thiophenemethylamino)-butanediamide

N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-methyl-propylamino)-butanediamide

The present invention also provides a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of formula (I) as described herein.

The present invention also provides for treating an inflammatory disease in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of formula (I) as described herein.

The present invention also provides a method for treating a condition or disease mediated by MMPs and/or TNF and/or aggrecanase in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of formula (I) as described herein.

The present invention alsoprovides a method for treating a condition or disease wherein the disease or condition is referred to as rheumatoid arthritis, osteoarthritis, periodontitis, gingivitis, corneal ulceration, solid tumor growth and tumor invasion by secondary metastases, neovascular glaucoma, multiple sclerosis, or psoriasis in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of formula (I) as described herein.

The present invention also provides a method for treating a condition or disease wherein the disease or condition is referred to as fever, cardiovascular effects, hemorrhage, coagulation, cachexia, anorexia, alcoholism, acute phase response, acute infection, shock, graft versus host reaction, autoimmune disease or HIV infection in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of formula (I) as described herein.

In the following description a (−) symbolizes the point of attachment.

SYNTHESIS

The novel compounds of the present invention may be prepared in a number of ways well known to one skilled in the art of organic synthesis. The compounds of the present invention can be synthesized using the methods described below, together with synthetic methods known in the art of synthetic organic chemistry, or variations thereon as appreciated by those skilled in the art. Preferred methods include, but are not limited to, those described below. All references cited herein are hereby incorporated in their entirety herein by reference.

The novel compounds of this invention may be prepared using the reactions and techniques in this section. The reactions are performed in solvents appropriate to the reagents and materials employed and suitable for the transformation being effected. Also, in the description of the synthetic methods described below, it is to be understood that all proposed reaction conditions, including choice of solvents, reaction temperature, duration of the experiment and workup procedures, are chosen to be the conditions standard for that reaction, which should be readily recognized by one skilled in the art. It is understood by one skilled in the art of organic synthesis that the functionality present on various portions of the molecule must be compatible with the reagents and reactions proposed. Such restrictions to the substituents which are compatible with the reaction conditions will be readily apparent to one skilled in the art and alternate methods must then be used.

A series of compounds of formula 5 are prepared by the methods outlined in scheme 1. Coupling of carboxylic acid 1 with cis-(1S,2R-(−)-1-amino-2-indanol provided amide 2. The hydroxyl group of 2 was protected as the acetonide 3, followed by alkylation with tert-butyl 2-bromo-acetate to afford the desired diastereomer 4. Removal of the tert-butyl group of 4 with TFA in methylene chloride, followed by coupling with O-benzyl hydroxy amine, and hydrogenation afforded the target molecule 5.

Compounds of formula 5 can also be prepared by the methods outlined in scheme 2. The 2-substituted succinic acid 10 can be prepared using standard Evans chemistry. An acid 6 (X=OH) is converted to its oxazolidinone derivative 8 using the standard chemistry. Asymmetric alkylation, followed by hydrolysis using H₂O₂/LiOH afforded the desired acid 10. The mono-protected succinic acid was coupled to (1S, 2R)-(−) cis-1-amino-2-indanol using standard BOP, or other peptide coupling reagents such as DCC, EDAC, TBTU. The intermediate 11 can then be readily converted into the target compounds 5 using the similar procedures to that used for the synthesis of target 5 as described in scheme 1.

Compounds of formula 12 are prepared by the methods outlined in scheme 3. Dianion reaction of the intermidate 10 with an organic halides or triflates produces the 2,3-disubstituted succinate 13. The acid 13 was coupled with cis-(1S, 2R)-(−)-1-amino-2-indanol. Following similar procedures to that used for the synthesis of target 5 as described in scheme 1, compounds of formula 12 can be readily prepared.

Compounds of formula 19 are prepared as shown in scheme 4. The intermediate 15 prepared using the method described in scheme 3, was hydrogenated to produce 16. Compound 16 was then converted to the triflate 17. The Pd catalyzed Suzuki or stille cross coupling of triflate 17 with either a boronic acid or organostanane afford the coupling product 18. Using the standard chemistry as described in scheme 3, 18 can be easily converted to the compounds of formula 19.

Compounds of formula 20 are prepared as shown in scheme 5. Compound 21 prepared as described in scheme 2 can be hydrogenated to give the free amine 22. The free amino group can then be protected as sulfonamides, carbamates, and amides 23. Following similar chemistry to that described in scheme 1, compound 23 can be readily converted to the target of formula 20.

Compounds of formula 24 are prepared as shown in scheme 6. Starting from 22 prepared in scheme 5, the free amino group can be further functionalized to afford compound 28 by either palladium catalyzed aryl amination (Wolfe, J. P.; Rennels, R. A.; Buchwald, S. L. Tetrahedron, 1996, 52, 7525-7546, Hartwig, J. F. Synlett, 1996, 329), or displacement with a substituted aryl fluoride. As described in the previous scheme 5, 28 can be easily converted to the final compound 24.

Compounds of formula 29 are prepared as shown in schemes 7-9.

The synthesis of substituted cis-1-amino-2-indanol (36) was followed by the route developed by Ghosh et al Ghosh, A. K.; Kincaid, J. F.; Haske, M. G. Synthesis, 1997, 541-544) The substituted indene (30) is converted to the epoxide 31 with MCPBA, or to the optically pure epoxide of 31 with Jacobsen's highly enantioselective epoxidation catalysts (Jacobsen, E. N.; Zhang, W.; Muci, A. R.; Ecker, J. R.; Deng, L. J. Am. Chem. Soc. 1991, 113, 7063-7064.). The epoxide 31 is converted to the alcohol 32 by treating it with NaN₃. The racemic alcohol of 32 is resolved by Lipase P Sas described by Ghosh et al (Ghosh, A. K.; Kincaid, J. F.; Haske, M. G. Synthesis, 1997, 541-544). The azide of 33 was hydrogenated in the presence of O(CO₂Et)₂ to give 34. The compound 34 was then converted to final substituted cis-1-amino-2-indanol 36 first by mixing with SOCl₂, followed by hydrolysis.

Alternatively, the substituted cis-1-amino-2-indanol 36 is directly prepared from substituted indene (30) following a method recently developed by Sharpless, K. B. et al as shown in scheme 8 (Li, G.; Angert, H. H.; Sharpless, K. B. Angew. Chem. Int. Ed. Engl. 1996, 35, 2813). The cbz group of 38 was removed by hydrogenation to give the free amine 36.

Following a similar sequence, the compound 36 can then be readily converted to the final compound 29 as shown in scheme 9.

Compounds of formula 39 can be synthesized as shown in scheme 10. Following the method developed by Sudo and Saigo (Sudo, A.; Saigo, K. Tetrahedron Asymetry, 1996, 7, 2939-2956), the racemic cis-2-amino-1-indanol can be readily synthesized from substituted indanone 40 as outlined in scheme 9. The indanone can be readily converted into oxime 41 with butyl nitrile under acidic conditions. Reduction of 41 with NaBH₄ in methanol could provide the hydroxy oxime, which was then treated with acetic anhydride and pyridine to give diacetate 42. Borane reduction of 42 then gives the racemic 43, which can then be directly used or resolved by co-crystalization with tartaric acid or others to provide the desired enantiomerically pure amine 43. Using similar chemistry to that used for the synthesis of target 5 as described in scheme 1, compound 44 can be readily converted to the target 39.

Compounds of formula 45 are synthesized as shown in scheme 11. The carboxylic group of commercially available aspartic acid was protected as methyl ester 47. Compound 47 was then treated with LiHMDS in THF at −78° C. to form the enolate, which was reacted with benzyl bromide to afford 48. The benzyl group of 48 was removed by hydrogenation. The resulting acid was then coupled with cis-2-amino indanol to give 49. Hydrolysis of compound 49, followed by coupling with hydroxy amine to furnish the desired target 45.

Compounds of formula 50 are synthesized as shown in scheme 12. Compound 51 was prepared using the similar procedure to that used for the synthesis of compound 49 (see scheme 11). The amino protecting group of 51 was removed by TFA in methylene chloride. The free amino group was converted to its corresponding amide, carbamate and sulfonamide 53 using the standard chemistry. Hydrolysis of compound 53, followed by coupling with hydroxy amine to furnish the desired target 50.

Compounds of formula 56 are synthesized as shown in scheme 13. The amino TFA salt 54 can be prepared as described in scheme 11 and scheme 12. The reductive amination of 54 with either ketone or aldehyde under the reducing agent of NaBH(OAc)3 provided the desired alkyl amine 55. The, benzyl or methyl group of 55 was removed by either hydrogenation or hydrolysis. The resulting acid was then coupled with hydroxy amine to furnish the desired target 56.

EXAMPLES

Abbreviations used in the Examples are defined as follows: “1×” for once, “2×” for twice, “3×” for thrice, “° C.” for degrees Celsius, “eq” for equivalent or equivalents, “g” for gram or grams, “mg” for milligram or milligrams, “mL” for milliliter or milliliters, “¹H” for proton, “h” for hour or hours, “M” for molar, “min” for minute or minutes, “MHz” for megahertz, “MS” for mass spectroscopy, “NMR” for nuclear magnetic resonance spectroscopy, “rt” for room temperature, “tlc” for thin layer chromatography, “v/v” for volume to volume ratio. “R” and “S” are stereochemical designations familiar to those skilled in the art.

Example 1 N1(2(R)-Hydroxy-1(S)-indanyl)-N-4-hydroxy-2(R)-isobutyl-butanediamide

(a) N1(2R-Hydroxy-1S-indanyl)-2R-isobutyl-3-(tert-butoxycarbonyl)propanamide:

To a stirred, cooled (0° C.) solution of 500 mg (2.17 mmol) 2R-isobutyl 3-(tert-butoxycarbonyl)propinoic acid and 323.9 mg (2.17 mmol) (1S, 2R)-(−) cis-1-amino-2-indanol in 4.0 mL of anhydrous DMF was added 731.4 mg of TBTU, followed by addition of 1.19 mL of diisopropylethyl amine. The reaction was allowed to warm to room temperature. After 1 h, the reaction mixture was diluted with 15 mL 10% citric acid and 50 mL ethyl acetate, the aqueous solution was further extracted with ethyl acetate (2×25 mL). The combined organic solution was washed with water, sat. NaHCO₃, and brine, dried over MgSO₄. The solution was filtered and concentrated under reduced pressure to afford 0.685 g (87% yield) as a white solid. ESI-MS (M+H)⁺: calcd 362, found 362.

(b) N-(2R-Hydroxy-1S-indanyl)-2R-isobutyl-3-(hydroxycarbonyl)propanamide:

To a solution of 0.635 g of N-(2R-hydroxy-1S-indanyl)-2R-isobutyl-3-(tert-butoxycarbonyl) propanamide in 4.5 mL methylene chloride and 0.5 mL water was dropwise added 5.0 mL of TFA. The reaction was stirred at room temperature for 50 min. The solution mixture was concentrated, and dried by co-evaporation with toluene (3×15 mL). The resulting material was directly used in the next step. ESI-MS (M+H)⁺: calcd 306, found 306.

(c) N1(2(R)-Hydroxy-1(S)-indanyl)-N-4-hydroxy-2(R)-isobutyl-butanediamide:

To a cooled (0° C.) solution of 501.0 mg of N-(2R-hydroxy-1S-indanyl)-2R-isobutyl-3-(hydroxycarbonyl) propanamide in 6.4 mL DMF was added 786.5 mg of O-benzyl hydroxyamine-HCl, and 684.6 mg of TBTU, followed by addition of 1.71 mL of ethyldiisopropyl amine. The reaction was stirred at 0° C. for 15 min. and warmed to room temperature. After 4 h, the reaction mixture was poured into ethyl acetate/5% citric acid, the aqueous solution was extracted with ethyl acetate (3×25 mL). The combined organic solution was washed with 5% citric acid, water, sat. NaHCO₃, brine, and dried over MgSO₄. The solution was filtered and concentrated to afford 647 mg of desired product as a white solid.

To 323.5 mg of the above in 20 mL methanol was added 500 mg of 5% Pd/BaSO₄. The mixture was shaken under 50 psi H₂ for 16 hours. The reaction mixture was filtered and concentrated and purified by reverse HPLC to afford 110 mg of the desired hydroxamic acid as a white solid. ESI-MS (M+H)⁺: calcd 321, found 321.

Example 2 N1(2(R)-Hydroxy-1(S)-indanyl)-N-4-hydroxy-2(R)-isobutyl-3(S)-(3-propionic Acid)-butanediamide

Following a procedure analogous to that used in example 1, 2R-isobutyl 3S-(tert-butoxycarbonyl) 5-benzoxycarbonyl pentanoic acid was coupled with (1S, 2R)-(−) cis-1-amino-2-indanol using TBTU as the coupling reagent. Removal of tert-butyl protecting group was achieved by treating with TFA as described in example 1, followed by coupling with O-benzyl hydroxyamine-HCl mediated by TBTU. The resulting material was hydrogenated to afford the desired product. ESI-MS (M+H)⁺: calcd 393, found 393.

Example 3 N1(2(R)-Hydroxy-1(S)-indanyl)-N-4-hydroxy-2(R)-isobutyl-3(S)-methyl-butanediamide

Following a procedure analogous to that used in example 1, 2R-hexyl 3S-(tert-butoxycarbonyl) butanoic acid was coupled with (1S, 2R)-(−) cis-1-amino-2-indanol using TBTU as the coupling reagent. Removal of tert-butyl protecting group was achieved by treating with TFA as described in example 1, followed by coupling with O-benzyl hydroxyamine-HCl mediated by TBTU or BOP. The resulting material was hydrogenated to afford the desired product as a white solid. ESI-MS (M+H)+: calcd 335, found 335.

Example 4 N1(2(R)-Hydroxy-1(S)-indanyl)-N-4-hydroxy-2(R)-isobutyl-3(S)-propyl-butanediamide

Following a procedure analogous to that used in example 1, 2R-isobutyl 3S-(tert-butoxycarbonyl) hexanoic acid was coupled with (1S, 2R)-(−) cis-1-amino-2-indanol using TBTU as the coupling reagent. Removal of tert-butyl protecting group was achieved by treating with TFA as described in example 1, followed by coupling with O-benzyl hydroxyamine-HCl mediated by TBTU or BOP. The resulting material was hydrogenated to afford the desired product as a white solid. ESI-MS (M+H)⁺: calcd 363, found 363.

Example 5 N1(2(R)-Hydroxy-1(S)-indanyl)-N-4-hydroxy-2(R)-hexyl-3(S)-propyl-butanediamide

Following a procedure analogous to that used in example 1, 2R-hexyl 3S-(tert-butoxycarbonyl) hexanoic acid was coupled with (1S, 2R)-(−) cis-1-amino-2-indanol using TBTU as the coupling reagent. Removal of tert-butyl protecting group was achieved by treating with TFA as described in example 1, followed by coupling with O-benzyl hydroxyamine-HCl mediated by TBTU or BOP. The resulting material was hydrogenated to afford the desired product as a white solid. ESI-MS (M+H)+: calcd 391, found 391.

Example 6 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[4-hydroxy-phenyl)methyl]-butanediamide

(a) Preparation of N-(2R-Hydroxy-1S-indanyl)-3-(4-benzyloxy-phenyl)-propanamide:

To a stirred, cooled (0° C.) solution of 10 g (39.1 mmol) 3-(4-benzyloxy-phenyl)-propinoic acid and 7 g (46.92 mmol) (1S, 2R)-(−) cis-1-amino-2-indanol in 200 mL of anhydrous DMF was added 17.3 g BOP as a solid, followed by addition of 20 mL of diethylisopropyl amine. The reaction was allowed to warm to room temperature. After 5 h, the reaction mixture was diluted with 100 mL 10% citric acid and 100 mL ethyl acetate, the aqueous solution was further extracted with ethyl acetate (2×50 mL). The combined organic solution was washed with water, sat. NaHCO₃, and brine, dried over MgSO₄. The solution was filtered and concentrated under reduced pressure to afford 15.1 g desired product as a white solid. ESI-MS (M+H)⁺: calcd 388, found 388.

(b) N-(1S,2R-N,O-Dimethyl Acetonide-indanyl)-3-(4-benzyloxy-phenyl)-propanamide:

To a stirred, cooled (0° C.) solution of 15.1 g N-(2R-hydroxy-1S-indanyl)-3-(4-benzyloxy-phenyl)-propanamide and 1.14 g of PPTS in 300 mL of methylene chloride was slowly added 30 ml of 2-methoxy propene. The solution was slowly warmed to room temperature and stirred overnight. The reaction was quenched by addition of 50 mL of sat. NaHCO₃, and extracted with ethyl acetate (3×50 mL). The combined solution was washed with sat NaHCO₃, water, brine, and dried over MgSO₄. The solution was filtered and concentrated. The crude material was purified by flash column (Ethyl acetate/Hexane: 40:60) to give 15.3 g desired product as a white solid. ESI-MS (M+H)⁺: calcd 428, found 428.

(c) N-(1S, 2R-N,O-Dimethyl Acetonide-indanyl)-2R-(4-benzyloxy-phenylmethyl)-3-(tert-butoxycarbonyl-propanamide:

To a stirred and cooled (−78° C.) solution of 3.0 g (7.0 mmol) of N-(2R-hydroxy-1S-indanyl)-3-(4-benzyloxy-phenyl)-propanamide in 20 mL THF was dropwise added a freshly prepared, cooled (−78° C.) LDA (7.0 mmol) in THF. After 1.0 hour, a solution of 1.14 mL (7.7 mmol) tert-butyl 2-bromoacetate in 3.0 ml THF was added dropwise. The resulting solution was incubated at −78° C. for 4.0 h. The reaction was quenched by addition of 10% citric acid, and extracted with ethyl acetate (3×100 mL). The combined organic solution was washed with water, brine, and dried over MgSO₄. The solution was filtered and concentrated. The crude material was purified by flash column with (Ethyl acetate/Hexane: 15-25:85-75) to afford the desired product (2.8 g, 71% yield) as a white solid, and 0.1 g of other diastereomer. ESI-MS (M+H)⁺: calcd 542, found 542.

(d) N-(2R-Hydroxy-1S-indanyl)-2R-(4-benzyloxy-phenylmethyl)-3-(hydroxy-carbonyl)propanamide:

To a solution of 1.13 g of N-(2R-hydroxy-1S-indanyl)-2R-(4-Benzyloxy-phenylmethyl)-3-(tert-butoxycarbonyl) propanamide in 7.6 mL methylene chloride and 0.4 mL water was dropwise added 8.0 mL of TFA. The reaction was stirred at room temperature for 50 min. The solution mixture was concentrated to half of its original volume. The residue was then dried by co-evaporation with toluene (3×15 mL) and directly used in the next step. ESI-MS (M+H)⁺: calcd 446, found 446.

(e) N-(2R-Hydroxy-1S-indanyl)-2K-(4-benzyloxy-phenylmethyl)-3-(N-hydroxyaminocarbonyl)propan-amide:

To a cooled (0° C.) solution of 104 mg of N-(2R-hydroxy-1S-indanyl)-2R-(4-Benzyloxy-phenylmethyl)-3-(hydroxy-carbonyl) propanamide in 1.2 mL DMF was added 112 mg of O-benzyl hydroxylamine-HCl, and 78.8 mg of TBTU, followed by addition of 0.24 mL of ethyldiisopropyl amine. The reaction was stirred at 0° C. for 15 min. and warmed to room temperature. After 2 h, the reaction mixture was poured into ethyl acetate/5% citric acid, the aqueous solution was extracted with ethyl acetate (3×25 mL). The combined organic solution was washed with 5% citric acid, water, sat. NaHCO₃, brine, and dried over MgSO₄. The solution was filtered and concentrated to afford 105 mg of desired product.

To 105 mg of the above in 6 mL methanol was added 60 mg of 5% Pd/BaSO₄. The mixture was shaken under 50 psi H₂ for 4 hour. The reaction mixture was filtered and concentrated and purified by reverse HPLC to afford 47 mg of the desired hydroxamic acid as a white solid. ESI-MS (M+H)⁺: calcd 371, found 371.

Example 7 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[4-methoxy-phenyl)methyl]-butanediamide

Prepared by the method described in example 6 to give the desired material. ESI-MS (M+H)⁺: calcd 385, found 385.

Example 8 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[4-(hydroxy-phenyl)methyl]-butanediamide

Prepared by the method described in example 6 to give the desired material. ESI-MS (M+H)⁺: calcd 355, found 355.

Example 9 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-phenyl-propyl]butanediamide

Prepared by the method described in example 6 to give the desired material. ESI-MS (M+H)⁺: calcd 383, found 383.

Example 10 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(benzyloxy)-phenyl]methyl]-butanediamide

Prepared by the method described in example 6 to give the desired material. ESI-MS (M+H)⁺: calcd 461, found 461.

Example 11 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[3-(benzyloxy)-phenyl]methyl]-butanediamide

Prepared by the method described in example 6 to give the desired material. ESI-MS (M+H)⁺: calcd 461, found 461.

Example 12 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[(3-(hydroxy-phenyl)methyl]-butanediamide

Prepared by the method described in example 6 to give the desired material. ESI-MS (M+H)⁺: calcd 371, found 371.

Example 13 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[4-(fluoro-phenyl)methyl]-butanediamide

Prepared by the method described in example 6 to give the desired material. ESI-MS (M+H) +: calcd 373, found 373.

Example 14 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3,4-(methylenedioxy-phenyl)methyl]-butanediamide

Prepared by the method described in example 6 to give the desired material. ESI-MS (M+H)⁺: calcd 379, found 379.

Example 15 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(methoxy-phenyl)methyl]-butanediamide

Prepared by the method described in example 6 to give the desired material. ESI-MS (M+H)⁺: calcd 385, found 385.

Example 16 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(phenyl)phenyl]methyl]-butanediamide

(a) N-(1S,2R-N,O-Dimethyl Acetonide-indanyl)-2R-(4-phenyl)phenylmethyl-3-(tert-butoxycarbonyl)propanamide

To 2.6 g N-(1S,2R-N,O-dimethyl acetonide-indanyl)-2R-(4-Benzyloxy-phenylmethyl)-3-(tert-butoxycarbonyl) propanamide in 20 mL methanol was added 300 mg of 5% Pd/C. The mixture was shaken under 50 psi H₂ for 17 hours. The reaction mixture was filtered and concentrated to afford 2.0 g of the desired product.

To a cooled (0° C.) solution of 1.2 g of N-(2R-hydroxy-1S-indanyl)-2R-(4-hydroxy-phenylmethyl)-3-(tert-butoxycarbonyl) propanamide and 0.95 g of PhN(tf)₂ in 9.0 mL of methylene chloride was dropwise added 0.77 mL Et₃N. After 45 min at 0° C., the reaction mixture was diluted in ethyl ether (60 mL), washed with sat NaHCO₃, brine, and dried over MgSO₄. The crude mater was purified by flash column with 20% ethyl acetate in hexane to afford the desired product as a colorless oil.

To a solution of 192.0 mg of above material and 22 mg of PPh₃ in 1.4 mL toluene and 1.4 mL 0.35M Na₂CO₃ aq. solution was added catalytical amount (6.0 mg) of Pd(Ac)₂. The resulting mixture was stirred at 60° C. for 10 min, followed by addition of 44 mg of benzene bornic acid as solid. The reaction was heated at 70° C. After four hours, the reaction mixture was then diluted with ethyl acetate, washed with water, brine, and dried over MgSO4. The crude material was purified by 15% ethyl acetate in hexane to afford 127.1 mg of desired product as a colorless oil. ESI-MS (M+H)⁺: calcd 431, found 431.

(b) N-(2R-Hydroxy-1S-indanyl)-2R-(4-phenyl)phenyl-methyl-3-(N-hydroxyaminocarbonyl)propanamide:

Following the method used in the synthesis of example 1, the above N-(1S ,2R-N,O-dimethyl acetonide-indanyl)-2R-(4-phenyl)phenylmethyl-3-(tert-butoxycarbonyl) propanamide was treated with TFA, followed by coupling with hydroxylamine to yield the desired N-(2R-hydroxy-1S-indanyl)-2R-(4-phenyl)-phenylmethyl-3-(N-hydroxyaminocarbonyl)-propanamide as a white solid. ESI-MS (M+H)⁺: calcd 431.2, found 431.2.

Example 17 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(2-tert-butylaminosulfonyl-phenyl)phenyl]methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 566, found 566.

Example 18 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(2-methoxy-phenyl)phenyl]methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 461, found 461.

Example 19 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(3-trifluoromethyl-phenyl)-phenyl]methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 499, found 499.

Example 20 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[(3-hydroxy-4-methylphenyl)-methyl]butanediamide

Prepared by the method described in example 6 to give the desired material. ESI-MS (M+H)⁺: calcd 401, found 401.

Example 21 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[3-(3-thiophene-isoxazoline]-methyl]butanediamide

Prepared by the method described in example 6 to give the desired material. ESI-MS (M+H)⁺: calcd 429, found 429.

Example 22 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(2-chloro-phenyl)-phenyl]-methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 465.5, found 465.5.

Example 23 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(2-benzofuran)-phenyl]-methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 471, found 471.

Example 24 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(2-methyl-phenyl)-phenyl]-methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 445, found 445.

Example 25 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[(3,4-(methylenedioxy-phenyl)-phenyl]methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 475, found 475.

Example 26 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(2-tetrazole-phenyl)-phenyl]-methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 499, found 499.

Example 27 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[3-phenyl)phenyl]methyl]-butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 431, found 431.

Example 28 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[3-methyl-phenyl)phenyl]methyl]-butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 445, found 445.

Example 29 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[4-(amino-phenyl)methyl]-butanediamide

Prepared by the method described in example 6 to give the desired material. ESI-MS (M+H)⁺: calcd 370, found 370.

Example 30 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[(4-(benzyloxy-carbonyl)-amino]phenyl)methyl]butanediamide

Prepared by the method described in example 6 to give the desired material. ESI-MS (M+H)⁺: calcd 504, found 504.

Example 31 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(2-hydroxymethlene)phenyl)-phenyl]methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 461, found 461.

Example 32 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(3,4,5-trimethoxy-phenyl)phenyl]methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 521, found 521.

Example 33 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(2,4-di-methoxy-phenyl)-phenyl]methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 491, found 491.

Example 34 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(3,5-di-chloro-phenyl)-phenyl]methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 499, found 499.

Example 35 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(2-trifluoromethyl-phenyl)-phenyl]methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 499, found 499.

Example 36 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(3-isopropyl-phenyl)-phenyl]methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 473, found 473.

Example 37 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(2,4-dichloro-phenyl)-phenyl]methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 499, found 499.

Example 38 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(3-chloro-4-fluoro-phenyl)-phenyl]methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 483, found 483.

Example 39 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(p-toluenesulfonylamino)-phenyl]methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 524, found 524.

Example 40 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-phenylmethyl-3(S)-(tert-butyloxy-carbonyl-amino)butanediamide

To a solution of 20 g of Boc-Asp(OBn)-OH and 8.9 g of K₂CO₃ in 200 mL DMF was added 4.04 mL of CH₃I. The reaction mixture was stirred at room temperature for 12 h. The mixture was diluted in water, extracted with diethyl ether. The combined organic layer was washed with sat. NaHCO₃, water and brine. The crude material was recrystalized from diethyl ether and hexane to afford 19.2 g of the desired product Boc-Asp(OBn)-OCH₃.

To a cooled (−78° C.) solution of 2.5 g of compound Boc-Asp(OBn)-OCH₃ in 49 mL toluene was added dropwise 15.2 mL of (1.0 M in THF) LiHMDS over 15 min. The resulting solution was stirred at −78° C. for 1.0 h, followed by addition of 1.4 mL benzyl bromide. The solution was stirred at −50° C overnight. The reaction was quenched with 10% citric acid, and extracted with diethyl ether. The organic layer was washed with sat. brine, dried over Na₂SO₄. The crude material was purified by 15% ethyl acetate to afford 2.1 g (64% yield) of desired product.

1.0 g (2.34 mmmol) above product and 500 mg of 10% Pd/C was hydrogenated at 32 Psi for two hour. The reaction mixture was filtered, and concentracted to afford a residue.

678 mg (2.01 mmol) above acid was coupled with 314 mg cis-2-amino indanol using 933 mg of BOP as the coupling reagent in DMF to afford 867 mg of coupling product N1-[2(R)-hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-phenylmethyl-3(S)-(tert-butyloxy-carbonyl-amino)-4-(tert-butoxycarbonyl)-butan-amide.

To a cooled solution of 268 mg of N1-[2(R)-hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-phenylmethyl-3(S)-(tert-butyloxy-carbonyl-amino)-4-(tert-butoxycarbonyl)butan-amide. in 4.3 mL THF was added 0.43 mL (2.5 M in H₂O) LiOH solution. The reaction mixture was stirred at 0° C. for 30 min. The reaction was quenched with 10% citric acid, extracted with EtOAc, the organic layer was washed with sat. brine, and dried over Na₂SO₄. The solvent was removed to afford 252.1 mg of the product as white solid.

The above acid (252 mg, 0.555 mmol) was treated with 257 mg of BOP and 116 mg of hydroxylamine in DMF. The crude material was purified by RP-HPLC (column: 41.5×250 mm C18 dynamax, gradient: 15 to 65% acetonitrile with 0.1% TFA over 25 min. The sample was detected at 220 nM.) to give the desired material N1-[2(R)-hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-phenylmethyl-3(S)-(tert-butyloxy-carbonyl-amino)-butanediamide, ESI-MS (M+H)⁺: calcd 470, found 470.

Example 41 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(3,4-methylenedioxyphenyl)-phenyl]methyl]-3(S)-(tert-butyloxy-carbonyl-amino)-butanediamide

Prepared by the method described in example 40 to give the desired material. ESI-MS (M+H)⁺: calcd 588, found 588.

Example 42 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(3-methoxyphenyl)-phenyl]methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 461, found 461.

Example 43 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(3-fluororphenyl)-phenyl]-methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 449, found 449.

Example 44 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(fluoro-phenyl)methyl]-3(S)-(tert-butyloxy-carbonyl-amino)-butanediamide

Prepared by the method described in example 40 to give the desired material. ESI-MS (M+H)⁺: calcd 488, found 488.

Example 45 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(tert-butyloxy-carbonyl-amino)-butanediamide

Prepared by the method described in example 40 to give the desired material. ESI-MS (M+H)⁺: calcd 486, found 486.

Example 46 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(3-nitrophenyl)phenyl]-methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 476, found 476.

Example 47 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[[4-(3-(methylsulfonyl-amino)-phenyl)phenyl]-methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 524, found 524.

Example 48 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2,2-dimethyl-propionamido)-butanediamide

Step 1: To a solution of 1.55 g of N1-[2(R)-hydroxy-1(S)-indanyl]-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(tert-butyloxy-carbonyl-amino)-Succinamic methyl ester was added 20 mL of 4N Hcl in dioxane at RT. The resulting solution was stirred at room temperature for 25 min. The reaction mixture was concentracted to afford 1.45 g of N1-[2(R)-hydroxy-1(S)-indanyl]-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-amino-Succinamic methyl ester as a white solid.

Step 2: To a ice cold solution of 166 mg (0.43 mmol) of N1-[2(R)-hydroxy-1(S)-indanyl]-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-amino-Succinamic methyl ester and 88 mg (0.86 mmol) of 2,2-dimethyl-propionic acid in 2.15 mL DMF was added 145 mg TBTU (0.45 mmol) as a solid, followed by addition of 0.23 mL of hunig base. The resulting solution was stirred at room temperature for two hours. The mixture was diluted in 5% NaHCO3 solution, and extracted with ethyl acetate (3×20 mL). The combined organic layer was washed with saturated brine, and dried with MgSO4. Flash column of the crude material with 50% ethyl acetate in hexane to give 189 mg (94% yield) of N1-[2(R)-hydroxy-1(S)-indanyl]-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2,2-dimethyl-propionamido)-Succinamic methyl ester as a off white solid.

Step 3: To a ice cold solution of 176 mg of N1-[2(R)-hydroxy-1(S)-indanyl]-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2,2-dimethyl-propionamido)-Succinamic methyl ester in 2.0 mL of THF was added 0.38 mL LiOH solution (2.5M). The resulting solutionon was stirred at 0° C. for 30 min. The reaction was quenched with 0.35 mL HCl (3N) solution, and extracted with ethyl acetate (3×10 mL). The combined solution was washed with saturated brine, dried over Na2SO4. The solution was then filterted and concentracted to afford 152 mg of N1-[2(R)-hydroxy-1(S)-indanyl]-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2,2-dimethyl-propionamido)-Succinamic acid as an off white solid.

Step 4: To an ice cold solution of 135 mg (0.297 mmol) of N1-[2(R)-hydroxy-1(S)-indanyl]-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2,2-dimethyl-propionamido)-Succinamic acid in 1.5 mL DMF was added 131 mg of BOP, followed by addition of 62 mg hydroxy amine and 0.15 mL hunig base. The resulting solution was stirred at room temperature for three hour. The crude material was directly purified on reverse-HPLC to afford 82 mg of the desired N1-[2(R)-hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2,2-dimethyl-propionamido)-butanediamide as white solid. ESI-MS (M+H)⁺: calcd 470, found 470.

Example 49 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(ethyloxy-carbonyl-amino)-butanediamide

Prepared by the method described in example 40 to give the desired material. ESI-MS (M+H)⁺: calcd 458, found 458.

Example 50 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(iso-butyloxy-carbonyl-amino)-butanediamide

Prepared by the method described in example 40 to give the desired material. ESI-MS (M+H)⁺: calcd 486, found 486.

Example 51 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(propionamido)-butanediamide

Prepared by the method described in example 40 to give the desired material. ESI-MS (M+H)⁺: calcd 458, found 458.

Example 52 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-methyl-cyclo-propane Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 40 to give the desired material. ESI-MS (M+H)⁺: calcd 452, found 452.

Example 53 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2,2-dimethyl-propyl-amino)-butanediamide

Step 1: A solution of 2.1 g of N1-[2(R)-hydroxy-1(S)-indanyl]-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-amino-Succinamic methyl ester in 18 mL 1,2-dichloroethane was mixed with 0.55 mL of pivaldehyde and 1.10 mL of hunig base for 20 min, followed by addition of 1.79 g of NaBH(OAc)3 as a solid. The resulting solution was stirred at room temperature for 3 hour. The reaction mixtur was diluted in 5% NaHCO3 and extracted with ethyl acetate (3×30 mL). The combined solution was washed with saturated brine. The crude material was purified on silica with 30-50% ethyl acetate in hexane to give 1.44 g of N1-[2(R)-hydroxy-1(S)-indanyl]-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2,2-dimethylpropyl-amino)-Succinamic methyl ester.

Step 2: To a ice cold solution of 290 mg of N1-[2(R)-hydroxy-1(S)-indanyl]-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2,2-dimethylpropyl-amino)-Succinamic methyl ester in 2.5 mL THF was added 0.63 mL of LiOH (2.5 M). The reaction mixture was stirred at 0° C. for 30 min. The reaction was quenched with 0.6 ml HCl solution (3N), tha mixture was then freeze dried.

Step 3: To an ice cold solution of above material in 1.5 mL DMF was added 295 mg of BOP, followed by addition of 264 mg hydroxyl amine and 0.8 mL hunig base. The resulting solution was stirred at room temperature for three hour. The crude material was directly purified on reverse-HPLC to afford 85 mg of the desired N1-[2(R)-hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2,2-dimethylpropyl-amino)-butanediamide as a white solid. ESI-MS (M+H)⁺: calcd 455, found 455.

Example 54 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(methylsulfonyl-amino)-butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 464, found 464.

Example 55 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-13-(hydroxy-phenyl)methyl]-3(S)-amino-butanediamide

Prepared by the method described in example 40 to give the desired material. ESI-MS (M+H)⁺: calcd 386, found 386.

Example 56 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[4-(methylsulfonylamino)-phenyl)methyl]butanediamide

Prepared by the method described in example 16 to give the desired material. ESI-MS (M+H)⁺: calcd 448, found 448.

Example 57 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(cyclobutane carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 468.5, found 468.5.

Example 58 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-hydroxymethyl-isobutanamide)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 486.5, found 486.5.

Example 59 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-1-hydroxyl-cyclopropane carboxyamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 470.5, found 470.5.

Example 60 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-phenyl-cycylopropane carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 530.6, found 530.6.

Example 61 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(bezene carboxamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 490.5, found 490.5.

Example 62 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-cyano-cyclopropane Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 479.5, found 479.5.

Example 63 N1-[2(R)-hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-phenyl-cyclopentane Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 558.6, found 558.6.

Example 64 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-methyl-cyclohexane Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 510.6, found 510.6.

Example 65 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-hydroxy-phenyl)methyl]-3(S)-2-indole Carboxamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 529.6, found 529.6.

Example 66 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-furan Carboxamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 480.5, found 480.5.

Example 67 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-quinoline Carboxamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 541.6, found 541.6.

Example 68 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(3,4,5-trimethoxy Benzene Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 580.6, found 580.6.

Example 69 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-methyl-3-amino-benzene Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 519.6, found 519.6.

Example 70 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-methyl-6-amino-benzene Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 519.6, found 619.6.

Example 71 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(3-pyridine Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 491.5, found 491.5.

Example 72 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-(2,4-dichloro-phenyl)-cyclopropane Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 599.6, found 599.6.

Example 73 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-(4-chloro-phenyl)-cyclopropane Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 565, found 565.

Example 74 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(3-methylsulfonyl)-benzene Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 568.6, found 568.6.

Example 75 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-methylsulfonyl-benzene Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 568.6, found 568.6.

Example 76 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(3-cyano-benzene Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 515.5, found 515.5.

Example 77 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(6-quinoline Carboxamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 541.6, found 541.6.

Example 78 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-ethyl, 3-Methyl-pyrazole 5-Carboxamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 522.6, found 522.6.

Example 79 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3-(4-morpholino-benzene Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 575.6, found 575.6.

Example 80 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-chloro-4-methylsulfonyl-benzene Carboxyamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 603, found 603.

Example 81 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(4-(imidazol-1-yl)benzene Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 556.6, found 556.6.

Example 82: N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-thiophene Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 496.6, found 496.6.

Example 83 N1-[2(R)-Hydroxy-1(S)-indanyl]-N-4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-tert-butyl, 3-Methyl-pyrazole 5-Carboxamido)-butanediamide

Prepared by the method described in example 40 to give the desired material. ESI-MS (M+H)⁺: calcd 550.6, found 550.6.

Example 84 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(4-aminomethyl benzene Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 519.6, found 519.6.

Example 85 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-hydroxyl-isobutanamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 472.6, found 472.6.

Example 86 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(cyclopropane Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 454.6, found 454.6.

Example 87 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(cyclopentane Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 482.6, found 482.6.

Example 88 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-cyclopentyl Acetamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 496.6, found 496.6.

Example 89 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(cyclohexane Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 496.6, found 496.6.

Example 90 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(4-(4-N-Boc-piperazinyl-1-yl)benzene Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 674.8, found 674.8.

Example 91 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-[4-(piperazinyl-1-yl)benzene Carboxamido-1-yl]-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 574.6, found 574.6.

Example 92 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-fluoro-6-chloro-benzene Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 542.9, found 542.9.

Example 93 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-amino-cyclohexane Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 511.6, found 511.6.

Example 94 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-methylthio-acetamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 474.6, found 474.6.

Example 95 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-methoxy-acetamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 458.5, found 458.5.

Example 96 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-allyl-cyclopentane Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 522.6, found 522.6.

Example 97 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-n-propyl-cyclopentane Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 524.6, found 524.6.

Example 98 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-allyl-cyclopropane Carboxamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 494.6, found 494.6.

Example 99 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(8-quinoline-sulfonamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 577.6, found 577.6.

Example 100 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(4-nitro-benzene Sulfonamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 571.6, found 571.6.

Example 101 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1,4-di-methyl-2-chloro-pyrazole-3-sulfonamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 579, found 579.

Example 102 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1,5-dimethyl-isooxazole 3-sulfonamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 545.6, found 545.6.

Example 103 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1-methyl-imidazole 3-sulfonamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 530.6, found 530.6.

Example 104 N1-[2(R)-(Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(benzene Sulfonamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 526.6, found 526.6.

Example 105 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(1,4-dimethyl Pyrazole 3-Sulfonamido)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 544.6, found 544.6.

Example 106 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-methylsulfonyl Benzene Sulfonamido-1-yl)-butanediamide

Prepared by the method described in example 48 to give the desired material. ESI-MS (M+H)⁺: calcd 604.7, found 604.7.

Example 107 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(cyclohexylamino)-butanediamide

Prepared by the method described in example 53 to give the desired material. ESI-MS (M+H)⁺: calcd 468, found 468.

Example 108 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(iso-propylamino)-butanediamide

Prepared by the method described in example 53 to give the desired material. ESI-MS (M+H)⁺: calcd 428, found 428.

Example 109 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[4(2-trifluoromethylphenyl)-phenylmethyl]-3(S)-(2,2-dimethylpropyl-amino)-butanediamide

Prepared by the method described in example 53 to give the desired material. ESI-MS (M+H)⁺: calcd 584, found 584.

Example 110 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(cyclopentylamino)-butanediamide

Prepared by the method described in example 53 to 10 give the desired material. ESI-MS (M+H)⁺: calcd 454.5, found 454.5.

Example 111 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(cyclopropylmethylamino)-butanediamide

Prepared by the method described in example 53 to give the desired material. ESI-MS (M+H)⁺: calcd 440.5, found 440.5.

Example 112 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(benzylamino)-butanediamide

Prepared by the method described in example 53 to give the desired material. ESI-MS (M+H)⁺: calcd 476.5, found 476.5.

Example 113 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-furanmethylamino)-butanediamide

Prepared by the method described in example 53 to give the desired material. ESI-MS (M+H)⁺: calcd 466.5, found 466.5.

Example 114 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-4-methylphenyl)methyl]-3(S)-(3-cyanophenylmethylamino)-butanediamide

Prepared by the method described in example 53 to give the desired material. ESI-MS (M+H)⁺: calcd 501.5, found 501.5.

Example 115 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-4-methylphenyl)methyl]-3(S)-(2,2-dimethylpropyl-amino)-butanediamide

Prepared by the method described in example 53 to give the desired material. ESI-MS (M+H)⁺: calcd 470.6, found 470.6.

Example 116 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-pentylamino)-butanediamide

Prepared by the method described in example 53 to give the desired material. ESI-MS (M+H)⁺: calcd 456.6, found 456.6.

Example 117 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(bis-cyclopropylmethyamino)-butanediamide

Prepared by the method described in example 53 to give the desired material. ESI-MS (M+H)⁺: calcd 494.6, found 494.6.

Example 118 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-thiophenemethylamino)-butanediamide

Prepared by the method described in example 53 to give the desired material. ESI-MS (M+H)⁺: calcd 482.6, found 482.6.

Example 119 N1-[2(R)-Hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-(hydroxy-phenyl)methyl]-3(S)-(2-methyl-propylamino)-butanediamide

Prepared by the method described in example 53 to give the desired material. ESI-MS (M+H)⁺: calcd 556.6, found 556.6.

TABLE 1

M + Ex # R₂ R₃ H 1 H iso-butyl 321 2 CH₂CH₂CO₂H iso-butyl 393 3 methyl iso-butyl 335 4 n-propyl iso-butyl 363 5 n-propyl n-C₆H₁₃ 391 6 H 4-hydroxyphenylmethyl 371 7 H 4-methoxyphenylmethyl 385 8 H 4-hydroxyphenylmethyl 355 9 H 3-phenylpropyl 383 10 H 4-benzyloxyphenylmethyl 461 11 H 3-benzyloxyphenylmethyl 461 12 H 3-hydroxyphenylmethyl 371 13 H 4-fluorophenylmethyl 373 14 H 3,4-methylenedioxy 379 phenylmethyl 15 H 3-methoxyphenylmethyl 385 16 H 4-phenyl-phenylmethyl 431 17 H 4-(2-(tert- 566 butylaminosulfonyl)- phenylphenylmethyl 18 H 4-(2-methoxyphenyl)- 461 phenylmethyl 19 H 4-(3-trifluoromethyl- 499 phenyl)-phenylmethyl 20 H (3-hydroxy-4- 401 methoxy)phenylmethyl 21 H 3-(3-thiophene)- 429 isoxazoline-methyl 22 H 4-(2-chlorophenyl)- 465 phenylmethyl 23 H 4-(2-benzofuran)- 471 phenylmethyl 24 H 4-(2-methylphenyl)-phenyl- 445 methyl 25 H (3,4-methylene- 475 dioxyphenyl)phenyl-methyl 26 H 4-(2-tetrazolephenyl)- 499 phenyl-methyl 27 H 3-phenylphenylmethyl 431 28 H (3-methyl-phenyl)- 445 phenylmethyl 29 H 4-amino-phenylmethyl 370 30 4-benzyloxy- 504 carbonyl-amino-phenylmethyl 31 H 4-(2-hydroxymethylene- 461 phenyl)phenylmethyl 32 H 4-(3,4,5-trimethoxy- 521 phenyl)phenylmethyl 33 H 4-(2,4-dimethoxy- 491 phenyl)phenylmethyl 34 H 4-(3,5-dichloro-phenyl)- 499 phenylmethyl 35 H 4-(2-trifluoromethyl- 499 phenyl)phenylmethyl 36 H 4-(3-isopropyl- 473 phenyl)phenyl-methyl 37 H 4-(2,4-dichloro- 499 phenyl)phenyl-methyl 38 H 4-(3-chloro,4-fluoro- 483 phenyl)phenylmethyl 39 H 4-(p-toluenesulfonyl- 524 amino)-phenylmethyl 40 BocNH phenylmethyl 470 41 BocNH 4-(3,4-methylenedioxy- 588 phenyl)phenylmethyl 42 H 4-(3-methoxy- 461 phenyl)phenylmethyl 43 H 4-(3-fluoro- 449 phenyl)phenylmethyl 44 BocNH 3-fluorophenylmethyl 488 45 BocNH 3-hydroxyphenylmethyl 486 46 H 4-(3-nitro- 476 phenyl)phenylmethyl 47 H 4-(3-methylsulfonylamino- 524 phenyl)phenylmethyl 48 2,2-dimethylpropionamido 3-hydroxyphenylmethyl 470 49 ethoxycarbonylamino 3-hydroxyphenylmethyl 458 50 iso-butoxy-carbonyl-amino 3-hydroxyphenylmethyl 486 51 propionamido 3-hydroxyphenylmethyl 458 52 1-methylcyclopropane 3-hydroxyphenylmethyl 452 carboxamido-1-yl 53 2,2-dimethylpropylamino 3-hydroxyphenylmethyl 455 54 methylsulfonylamino 3-hydroxyphenylmethyl 464 55 amino 3-hydroxyphenylmethyl 386 56 H 4-(methylsulfonyl- 448 amino)phenylmethyl 57 cyclobutane carboxamido- 3-hydroxyphenylmethyl 468.5 1-yl 58 2-hydroxymethyl- 3-hydroxyphenylmethyl 486.5 isobutanamide 59 1-hydroxyl-cyclopropane 3-hydroxyphenylmethyl 470.5 carboxyamido-1-yl 60 1-phenyl-cyclopropane 3-hydroxyphenylmethyl 530.6 carboxamido-1-yl 61 bezene carboxamido 3-hydroxyphenylmethyl 490.5 62 1-cyano-cyclopropane 3-hydroxyphenylmethyl 479.5 carboxamido-1-yl 63 1-phenyl-cyclopentane 3-hydroxyphenylmethyl 558.6 carboxamido-1-yl 64 1-methyl-cyclohexane 3-hydroxyphenylmethyl 510.6 carboxamido-1-yl 65 2-indole carboxamido 3-hydroxyphenylmethyl 529.6 66 2-furan carboxamido 3-hydroxyphenylmethyl 480.5 67 2-quinoline carboxamido 3-hydroxyphenylmethyl 541.6 68 3,4,5-trimethoxy benzene 3-hydroxyphenylmethyl 580.6 carboxamido-1-yl 69 2-methyl-3-amino-benzene 3-hydroxyphenylmethyl 519.6 carboxamido-1-yl 70 2-methyl-6-amino-benzene 3-hydroxyphenylmethyl 619.6 carboxamido-1-yl 71 3-pyridine carboxamido-1- 3-hydroxyphenylmethyl 491.5 yl 72 1-(2,4-dichloro-phenyl)- 3-hydroxyphenylmethyl 599.6 cyclopropane carboxamido- 1-yl 73 1-(4-chloro-phenyl)- 3-hydroxyphenylmethyl 565 cyclopropane carboxamido- 1-yl 74 3-methylsulfonyl)-benzene 3-hydroxyphenylmethyl 568.6 carboxamido-1-yl 75 2-methylsulfonyl-benzene 3-hydroxyphenylmethyl 568.6 carboxamido-1-yl 76 3-cyano-benzene 3-hydroxyphenylmethyl 515.6 carboxamido-1-yl 77 6-quinoline carboxamido 3-hydroxyphenylmethyl 541.6 78 1-ethyl,3-methyl-pyrazole 3-hydroxyphenylmethyl 522.6 5-carboxamido 79 4-morpholino-benzene 3-hydroxyphenylmethyl 575.6 carboxamido-1-yl 80 2-chloro-4-methylsulfonyl- 3-hydroxyphenylmethyl 603 benzene carboxamido-1-yl 81 4-(imidazol-1-yl)benzene 3-hydroxyphenylmethyl 556.6 carboxamido-1-yl 82 2-thiophene carboxamido- 3-hydroxyphenylmethyl 496.6 1-yl 83 1-tert-butyl,3-methyl- 3-hydroxyphenylmethyl 550.6 pyrazole 5-carboxamido 84 4-aminomethyl benzene 3-hydroxyphenylmethyl 519.6 carboxamido-1-yl 85 2-hydroxyl-isobutanamido 3-hydroxyphenylmethyl 472.6 86 cyclopropane carboxamido- 3-hydroxyphenylmethyl 454.6 1-yl 87 cyclopentane carboxamido- 3-hydroxyphenylmethyl 482.6 1-yl 88 2-cyclopentyl acetamido 3-hydroxyphenylmethyl 496.6 89 cyclohexane carboxamido- 3-hydroxyphenylmethyl 496.6 1-yl 90 4-(4-N-Boc-piperazinyl-1- 3-hydroxyphenylmethyl 674.8 yl)benzene carboxamido-1- yl 91 4-(piperazinyl-1- 3-hydroxyphenylmethyl 574.6 yl)benzene carboxamido-1- yl 92 2-Fluoro-6-chloro-benzene 3-hydroxyphenylmethyl 542.6 carboxamido-1-yl 93 1-amino-cyclohexane 3-hydroxyphenylmethyl 511.6 carboxamido-1-yl 94 2-methylthio-acetamido 3-hydroxyphenylmethyl 474.6 95 2-methoxy-acetamido 3-hydroxyphenylmethyl 458.5 96 1-allyl-cyclopentane 3-hydroxyphenylmethyl 522.6 carboxamido-1-yl 97 1-n-propyl-cyclopentane 3-hydroxyphenylmethyl 524.6 carboxamido-1-yl 98 1-allyl-cyclopropane 3-hydroxyphenylmethyl 494.6 carboxamido-1-yl 99 8-quinoline-sulfonamido 3-hydroxyphenylmethyl 577.6 100 4-nitro-benzene 3-hydroxyphenylmethyl 571.6 sulfonamido 101 1,4-di-methyl-2-chloro- 3-hydroxyphenylmethyl 579 pyrazole-3-sulfonamido 102 1,5-dimethyl-isooxazole 3- 3-hydroxyphenylmethyl 545.6 sulfonamido 103 1-methyl-imidazole 3- 3-hydroxyphenylmethyl 530.6 sulfonamido 104 benzene sulfonamido 3-hydroxyphenylmethyl 526.6 105 1,4-dimethyl pyrazole 3- 3-hydroxyphenylmethyl 544.6 sulfonamido 106 2-methylsulfonyl benzene 3-hydroxyphenylmethyl 604.7 sulfonamido-1-yl 107 cyclohexylamino 3-hydroxyphenylmethyl 468 108 iso-propylamino 3-hydroxyphenylmethyl 428 109 2,2-dimethylpropyl-amino 3-hydroxyphenylmethyl 584 110 cyclopentylamino 3-hydroxyphenylmethyl 454.5 111 cyclopropylmethylamino 3-hydroxyphenylmethyl 440.5 112 benzylamine 3-hydroxyphenylmethyl 476.5 113 2-furanmethylamino 3-hydroxyphenylmethyl 466.5 114 3-cyanophenylmethylamino 3-hydroxyphenylmethyl 501.5 115 2,2-dimethylpropyl-amino 3-(hydroxy-4- 470.6 methylphenyl)methyl 116 2-pentylamino 3-hydroxyphenylmethyl 456.6 117 bis-cyclopropylmethyamino 3-hydroxyphenylmethyl 494.6 118 2-thiophenemethylamino 3-hydroxyphenylmethyl 482.6 119 2-methyl-propylamino 3-hydroxyphenylmethyl 556.6

The following tables contain representative examples of the present invention. Each entry in each table is intended to be paired with the formula at the start of the table.

TABLE 2

I

II

III

IV

V

VI

VII

VIII

IX

X

XI

XII

XIII

XIV

XV

XVI

XVII

XVIII

XIX

XX

XXI

XXII

XXIII

XXIV

XXV

XXVI

XXVII

XXVIII

XXIX

XXX

XXXI

XXXII Ex # R2 R3 Ms 200 H H 201 H methyl 202 H ethyl 203 H n-propyl 204 H n-butyl 205 H n-pentyl 206 H n-hexanyl 207 H n-heptanyl 208 H isopropyl 209 H tert-butyl 210 H cyclopropyl 211 H cyclobutanyl 212 H cyclopentanyl 213 H cyclohexanyl 214 H cycloheptanyl 215 H phenyl 216 H phenylmethyl 217 H 3-hydroxyphenyl 218 H 3-hydroxy-4-methoxyphenyl 219 H 3-fluorophenyl 220 H 3-chlorophenyl 221 H 3-nitrophenyl 222 H 3-aminophenyl 223 H 3-methylsulfonamidephenyl 224 H 3-trifluoro- methylsulfonamidephenyl 225 H 3-Ac—NHphenyl 226 H 3-Boc—NHphenyl 227 H 3-Cbz—NHphenyl 228 H 3-aminomethylenephenyl 229 H 3-aminoethylenephenyl 230 H 3-cyanophenyl 231 H 3-cyanomethylphenyl 232 H 3-hydroxymethylenephenyl 233 H 3-carboxylphenyl 234 H 3-mercaptophenyl 235 H 3-methoxyphenyl 236 H 3,4-methylenedioxophenyl 237 H 3-tetrazolephenyl 238 H 3-aminosulfonylphenyl 239 H 3-methylamino- sulfonylphenyl 240 H 3-ethylamino-sulfonylphenyl 241 H 3-tert-butylamino- sulfonylphenyl 242 H 3-methylsulfonylphenyl 243 H 4-methoxyphenyl 244 H 4-phenylphenyl 245 H (2-hydroxy- methylenephenyl)-phenyl 246 H (2-tert-butylamino- sufonylphenyl)-phenyl 247 H (2-methylamino- sufonylphenyl)-phenyl 248 H (2-ethylamino- sufonylphenyl)-phenyl 249 H (2-amino-sufonylphenyl)- phenyl 250 H (2-chlorophenyl)-phenyl 251 H (2-fluorophenyl)-phenyl 252 H (2,4-dichlorophenyl)-phenyl 253 H (2,6-dichlorophenyl)-phenyl 254 H (3,5-dichlorophenyl)-phenyl 256 H (2,3-dichlorophenyl)-phenyl 257 H (2-methylphenyl)-phenyl 258 H (2-tetrazole-phenyl)-phenyl 259 H (2-methoxy-phenyl)-phenyl 260 H (2-tmethyl-phenyl)-phenyl 261 H (2-formyl-phenyl)-phenyl 262 H (2-amino-phenyl)-phenyl 263 H (2-methylamino-phenyl)- phenyl 264 H (2-ethylamino-phenyl)- phenyl 265 H (2-propylamino-phenyl)- phenyl 266 H (2-methylsulfonylamino- phenyl)-phenyl 267 H (2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 268 H (3-methylphenyl)-phenyl 269 H (3-isopropylphenyl)-phenyl 270 H (3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 271 H (3-methylsulfonylamino- phenyl)-phenyl 272 H (3-amino-phenyl)-phenyl 273 H (3-nitro-phenyl)-phenyl 274 H 2-pyridyl 275 H 3-pyridyl 276 H 4-pyridyl 277 H 3-amino-4-pyridyl 278 H 3-hydroxy-4-pyridyl 279 H 3-imidazole 280 H 2-nitro-3-imidazole 281 H 5-thiazole 282 H 5-oxazole 283 H 4-pyazole 284 H phenylethyl 285 H 2-aminophenylethyl 286 H 2-methylsulfonylamino- phenylethyl 287 H 2-trifluoromethylsulfonyl- amino-phenylethyl 288 H 2-hydroxymethylene- phenylethyl 289 H 2-aminomethylene- phenylethyl 290 H 2-tetrazolephenylethyl 291 H 2-tert-butylamino- sulfonylphenylethyl 292 H 2-aminosulfonyl-phenylethyl 293 H 2-methoxyphenylethyl 294 H 3-aminophenylethyl 295 H 3-methylsulfonylamino- phenylethyl 296 H 3-trifluoromethylsulfonyl- amino-phenylethyl 297 H 3-hydroxymethylene- phenylethyl 298 H 3-aminomethylene- phenylethyl 299 H 3-tetrazolephenylethyl 300 H 3-tert-butylamino- sulfonylphenylethyl 301 H 3-aminosulfonyl-phenylethyl 302 H 3-methoxyphenylethyl 303 methyl H 304 methyl methyl 305 methyl ethyl 306 methyl n-propyl 307 methyl n-butyl 308 methyl n-pentyl 309 methyl n-hexanyl 310 methyl n-heptanyl 311 methyl isopropyl 312 methyl tert-butyl 313 methyl cyclopropyl 314 methyl cyclobutanyl 315 methyl cyclpentanyl 316 methyl cyclohexanyl 317 methyl cycloheptanyl 318 methyl phenyl 319 methyl phenylmethyl 320 methyl 3-hydroxyphenyl 321 methyl 3-hydroxy-4-methoxyphenyl 322 methyl 3-fluorophenyl 323 methyl 3-chlorophenyl 324 methyl 3-nitrophenyl 325 methyl 3-aminophenyl 326 methyl 3-methylsulfonamidephenyl 327 methyl 3-trifluoro- methylsulfonamidephenyl 328 methyl 3-Ac—NHphenyl 329 methyl 3-Boc—NHphenyl 330 methyl 3-Cbz—NHphenyl 331 Methyl 3-aminomethylenephenyl 332 methyl 3-aminoethylenephenyl 333 methyl 3-cyanophenyl 334 methyl 3-cyanomethylphenyl 335 methyl 3-hydroxymethylenephenyl 336 methyl 3-carboxylphenyl 337 methyl 3-mercaptophenyl 338 methyl 3-methoxyphenyl 339 methyl 3,4-methylenedioxophenyl 340 methyl 3-tetrazolephenyl 341 methyl 3-aminosulfonylphenyl 342 methyl 3-methylamino- sulfonylphenyl 343 methyl 3-ethylamino-sulfonylphenyl 344 methyl 3-tert-butylamino- sulfonylphenyl 345 methyl 3-methylsulfonylphenyl 346 methyl 4-methoxyphenyl 347 methyl 4-phenylphenyl 348 methyl (2-hydroxy- methylenephenyl)-phenyl 349 methyl (2-tert-butylamino- sufonylphenyl)-phenyl 350 methyl (2-methylamino- sufonylphenyl)-phenyl 351 methyl (2-ethylamino- sufonylphenyl)-phenyl 352 methyl (2-aminosufonyl-phenyl)- phenyl 353 methyl (2-chlorophenyl)-phenyl 354 methyl (2-fluorophenyl)-phenyl 355 methyl (2,4-dichlorophenyl)-phenyl 356 methyl (2,6-dichlorophenyl)-phenyl 357 methyl (3,5-dichlorophenyl)-phenyl 358 methyl (2,3-dichlorophenyl)-phenyl 359 methyl (2-methylphenyl)-phenyl 360 methyl (2-tetrazole-phenyl)-phenyl 361 methyl (2-methoxy-phenyl)-phenyl 362 methyl (2-tmethyl-phenyl)-phenyl 363 methyl (2-formyl-phenyl)-phenyl 364 methyl (2-amino-phenyl)-phenyl 365 methyl (2-methylamino-phenyl)- phenyl 366 methyl (2-ethylamino-phenyl)- phenyl 367 methyl (2-propylamino-phenyl)- phenyl 368 methyl (2-methylsulfonylamino- phenyl)-phenyl 369 methyl (2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 370 methyl (3-methylphenyl)-phenyl 371 methyl (3-isopropylphenyl)-phenyl 372 methyl (3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 373 methyl (3-methylsulfonylamino- phenyl)-phenyl 374 methyl (3-amino-phenyl)-phenyl 375 methyl (3-nitro-phenyl)-phenyl 376 methyl 2-pyridyl 377 methyl 3-pyridyl 378 methyl 4-pyridyl 379 methyl 3-amino-4-pyridyl 380 methyl 3-hydroxy-4-pyridyl 381 methyl 3-imidazole 382 methyl 2-nitro-3-imidazole 383 methyl 5-thiazole 384 methyl 5-oxazole 385 methyl 4-pyazole 386 methyl phenylethyl 387 methyl 2-aminophenylethyl 388 methyl 2-methylsulfonylamino- phenylethyl 389 methyl 2-trifluoromethylsulfonyl- amino-phenylethyl 390 methyl 2-hydroxymethylene- phenylethyl 391 methyl 2-aminomethylene- phenylethyl 392 methyl 2-tetrazolephenylethyl 393 methyl 2-tert-butylamino- sulfonylphenylethyl 394 methyl 2-aminosulfonyl-phenylethyl 395 methyl 2-methoxyphenylethyl 396 methyl 3-aminophenylethyl 397 methyl 3-methylsulfonylamino- phenylethyl 398 methyl 3-trifluoromethylsulfonyl- amino-phenylethyl 399 methyl 3-hydroxymethylene- phenylethyl 400 methyl 3-aminomethylene- phenylethyl 401 methyl 3-tetrazolephenylethyl 402 methyl 3-tert-butylamino- sulfonylphenylethyl 403 methyl 3-aminosulfonyl-phenylethyl 404 methyl 3-methoxyphenylethyl 405 OH H 406 OH methyl 407 OH ethyl 408 OH n-propyl 409 OH n-butyl 410 OH n-pentyl 411 OH n-hexanyl 412 OH n-heptanyl 413 OH isopropyl 414 OH tert-butyl 415 OH cyclopropyl 416 OH cyclobutanyl 417 OH cyclpentanyl 418 OH cyclohexanyl 419 OH cycloheptanyl 420 OH phenyl 421 OH phenylmethyl 422 OH 3-hydroxyphenyl 423 OH 3-hydroxy-4-methoxyphenyl 424 OH 3-fluorophenyl 425 OH 3-chlorophenyl 426 OH 3-nitrophenyl 427 OH 3-aminophenyl 428 OH 3-methylsulfonamidephenyl 429 OH 3-trifluoro- methylsulfonamidephenyl 430 OH 3-Ac—NHphenyl 431 OH 3-Boc—NHphenyl 432 OH 3-Cbz—NHphenyl 433 OH 3-aminomethylenephenyl 434 OH 3-aminoethylenephenyl 435 OH 3-cyanophenyl 436 OH 3-cyanomethylphenyl 437 OH 3-hydroxymethylenephenyl 438 OH 3-carboxylphenyl 439 OH 3-mercaptophenyl 440 OH 3-methoxyphenyl 441 OH 3,4-methylenedioxophenyl 442 OH 3-tetrazolephenyl 443 OH 3-aminosulfonylphenyl 444 OH 3-methylamino- sulfonylphenyl 445 OH 3-ethylamino-sulfonylphenyl 446 OH 3-tert-butylamino- sulfonylphenyl 447 OH 3-methylsulfonylphenyl 448 OH 4-methoxyphenyl 449 OH 4-phenylphenyl 450 OH (2-hydroxy- methylenephenyl)-phenyl 451 OH (2-tert-butylamino- sufonylphenyl)-phenyl 452 OH (2-methylamino- sufonylphenyl)-phenyl 453 OH (2-ethylamino- sufonylphenyl)-phenyl 454 OH (2-aminosufonyl-phenyl)- phenyl 455 OH (2-chlorophenyl)-phenyl 456 OH (2-fluorophenyl)-phenyl 457 OH (2,4-dichlorophenyl)-phenyl 458 OH (2,6-dichlorophenyl)-phenyl 459 OH (3,5-dichlorophenyl)-phenyl 460 OH (2,3-dichlorophenyl)-phenyl 461 OH (2-methylphenyl)-phenyl 462 OH (2-tetrazole-phenyl)-phenyl 463 OH (2-methoxy-phenyl)-phenyl 464 OH (2-tmethyl-phenyl)-phenyl 465 OH (2-formyl-phenyl)-phenyl 466 OH (2-amino-phenyl)-phenyl 467 OH (2-methylamino-phenyl)- phenyl 468 OH (2-ethylamino-phenyl)- phenyl 469 OH (2-propylamino-phenyl)- phenyl 470 OH (2-methylsulfonylamino- phenyl)-phenyl 471 OH (2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 472 OH (3-methylphenyl)-phenyl 473 OH (3-isopropylphenyl)-phenyl 474 OH (3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 475 OH (3-methylsulfonylamino- phenyl)-phenyl 476 OH (3-amino-phenyl)-phenyl 477 OH (3-nitro-phenyl)-phenyl 478 OH 2-pyridyl 479 OH 3-pyridyl 480 OH 4-pyridyl 481 OH 3-amino-4-pyridyl 482 OH 3-hydroxy-4-pyridyl 483 OH 3-imidazole 484 OH 2-nitro-3-imidazole 485 OH 5-thiazole 486 OH 5-oxazole 487 OH 4-pyazole 488 OH phenylethyl 489 OH 2-aminophenylethyl 490 OH 2-methylsulfonylamino- phenylethyl 491 OH 2-trifluoromethylsulfonyl- amino-phenylethyl 492 OH 2-hydroxymethylene- phenylethyl 493 OH 2-aminomethylene- phenylethyl 494 OH 2-tetrazolephenylethyl 495 OH 2-tert-butylamino- sulfonylphenylethyl 496 OH 2-aminosulfonyl-phenylethyl 497 OH 2-methoxyphenylethyl 498 OH 3-aminophenylethyl 499 OH 3-methylsulfonylamino- phenylethyl 500 OH 3-trifluoromethylsulfonyl- amino-phenylethyl 501 OH 3-hydroxymethylene- phenylethyl 502 OH 3-aminomethylene- phenylethyl 503 OH 3-tetrazolephenylethyl 504 OH 3-tert-butylamino- sulfonylphenylethyl 505 OH 3-aminosulfonyl-phenylethyl 506 OH 3-methoxyphenylethyl 507 NH(CO)CH₃ H 508 NH(CO)CH₃ methyl 509 NH(CO)CH₃ ethyl 510 NH(CO)CH₃ n-propyl 511 NH(CO)CH₃ n-butyl 512 NH(CO)CH₃ n-pentyl 513 NH(CO)CH₃ n-hexanyl 514 NH(CO)CH₃ n-heptanyl 515 NH(CO)CH₃ isopropyl 516 NH(CO)CH₃ tert-butyl 517 NH(CO)CH₃ cyclopropyl 518 NH(CO)CH₃ cyclobutanyl 519 NH(CO)CH₃ cyclpentanyl 520 NH(CO)CH₃ cyclohexanyl 521 NH(CO)CH₃ cycloheptanyl 522 NH(CO)CH₃ phenyl 523 NH(CO)CH₃ phenylmethyl 524 NH(CO)CH₃ 3-hydroxyphenyl 525 NH(CO)CH₃ 3-hydroxy-4-methoxyphenyl 526 NH(CO)CH₃ 3-fluorophenyl 527 NH(CO)CH₃ 3-chlorophenyl 528 NH(CO)CH₃ 3-nitrophenyl 529 NH(CO)CH₃ 3-aminophenyl 530 NH(CO)CH₃ 3-methyl-sulfonamidephenyl 531 NH(CO)CH₃ 3-trifluoro- methylsulfonamidephenyl 532 NH(CO)CH₃ 3-Ac—NHphenyl 533 NH(CO)CH₃ 3-Boc—NHphenyl 534 NH(CO)CH₃ 3-Cbz—NHphenyl 535 NH(CO)CH₃ 3-aminomethylenephenyl 536 NH(CO)CH₃ 3-aminoethylenephenyl 537 NH(CO)CH₃ 3-cyanophenyl 538 NH(CO)CH₃ 3-cyanomethylphenyl 539 NH(CO)CH₃ 3-hydroxymethylenephenyl 540 NH(CO)CH₃ 3-carboxylphenyl 541 NH(CO)CH₃ 3-mercaptophenyl 542 NH(CO)CH₃ 3-methoxyphenyl 543 NH(CO)CH₃ 3,4-methylenedioxophenyl 544 NH(CO)CH₃ 3-tetrazolephenyl 545 NH(CO)CH₃ 3-aminosulfonylphenyl 546 NH(CO)CH₃ 3-methylamino- sulfonylphenyl 547 NH(CO)CH₃ 3-ethylamino-sulfonylphenyl 548 NH(CO)CH₃ 3-tert-butylamino- sulfonylphenyl 549 NH(CO)CH₃ 3-methylsulfonylphenyl 550 NH(CO)CH₃ 4-methoxyphenyl 551 NH(CO)CH₃ 4-phenylphenyl 552 NH(CO)CH₃ (2-hydroxy- methylenephenyl)-phenyl 553 NH(CO)CH₃ (2-tert-butylamino- sufonylphenyl)-phenyl 554 NH(CO)CH₃ (2-methylamino- sufonylphenyl)-phenyl 555 NH(CO)CH₃ (2-ethylamino- sufonylphenyl)-phenyl 556 NH(CO)CH₃ (2-aminosufonyl-phenyl)- phenyl 557 NH(CO)CH₃ (2-chlorophenyl)-phenyl 558 NH(CO)CH₃ (2-fluorophenyl)-phenyl 559 NH(CO)CH₃ (2,4-dichlorophenyl)-phenyl 560 NH(CO)CH₃ (2,6-dichlorophenyl)-phenyl 561 NH(CO)CH₃ (3,5-dichlorophenyl)-phenyl 562 NH(CO)CH₃ (2,3-dichlorophenyl)-phenyl 563 NH(CO)CH₃ (2-methylphenyl)-phenyl 564 NH(CO)CH₃ (2-tetrazole-phenyl)-phenyl 565 NH(CO)CH₃ (2-methoxy-phenyl)-phenyl 566 NH(CO)CH₃ (2-tmethyl-phenyl)-phenyl 567 NH(CO)CH₃ (2-formyl-phenyl)-phenyl 568 NH(CO)CH₃ (2-amino-phenyl)-phenyl 569 NH(CO)CH₃ (2-methylamino-phenyl)- phenyl 570 NH(CO)CH₃ (2-ethylamino-phenyl)- phenyl 571 NH(CO)CH₃ (2-propylamino-phenyl)- phenyl 572 NH(CO)CH₃ (2-methylsulfonylamino- phenyl)-phenyl 573 NH(CO)CH₃ (2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 574 NH(CO)CH₃ (3-methylphenyl)-phenyl 575 NH(CO)CH₃ (3-isopropylphenyl)-phenyl 576 NH(CO)CH₃ (3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 577 NH(CO)CH₃ (3-methylsulfonylamino- phenyl)-phenyl 578 NH(CO)CH₃ (3-amino-phenyl)-phenyl 579 NH(CO)CH₃ (3-nitro-phenyl)-phenyl 580 NH(CO)CH₃ 2-pyridyl 581 NH(CO)CH₃ 3-pyridyl 582 NH(CO)CH₃ 4-pyridyl 583 NH(CO)CH₃ 3-amino-4-pyridyl 584 NH(CO)CH₃ 3-hydroxy-4-pyridyl 585 NH(CO)CH₃ 3-imidazole 586 NH(CO)CH₃ 2-nitro-3-imidazole 587 NH(CO)CH₃ 5-thiazole 588 NH(CO)CH₃ 5-oxazole 589 NH(CO)CH₃ 4-pyazole 590 NH(CO)CH₃ phenylethyl 591 NH(CO)CH₃ 2-aminophenylethyl 592 NH(CO)CH₃ 2-methylsulfonylamino- phenylethyl 593 NH(CO)CH₃ 2-trifluoromethylsulfonyl- amino-phenylethyl 594 NH(CO)CH₃ 2-hydroxymethylene- phenylethyl 595 NH(CO)CH₃ 2-aminomethylene- phenylethyl 596 NH(CO)CH₃ 2-tetrazolephenylethyl 597 NH(CO)CH₃ 2-tert-butylamino- sulfonylphenylethyl 598 NH(CO)CH₃ 2-aminosulfonyl-phenylethyl 599 NH(CO)CH₃ 2-methoxyphenylethyl 600 NH(CO)CH₃ 3-aminophenylethyl 601 NH(CO)CH₃ 3-methylsulfonylamino- phenylethyl 602 NH(CO)CH₃ 3-trifluoromethylsulfonyl- amino-phenylethyl 603 NH(CO)CH₃ 3-hydroxymethylene- phenylethyl 604 NH(CO)CH₃ 3-aminomethylene- phenylethyl 605 NH(CO)CH₃ 3-tetrazolephenylethyl 606 NH(CO)CH₃ 3-tert-butylamino- sulfonylphenylethyl 607 NH(CO)CH₃ 3-aminosulfonyl-phenylethyl 608 NH(CO)CH₃ 3-methoxyphenylethyl 609 610 NH(CO)C₂H₅ H 611 NH(CO)C₂H₅ methyl 612 NH(CO)C₂H₅ ethyl 613 NH(CO)C₂H₅ n-propyl 614 NH(CO)C₂H₅ n-butyl 615 NH(CO)C₂H₅ n-pentyl 616 NH(CO)C₂H₅ n-hexanyl 617 NH(CO)C₂H₅ n-heptanyl 618 NH(CO)C₂H₅ isopropyl 619 NH(CO)C₂H₅ tert-butyl 620 NH(CO)C₂H₅ cyclopropyl 621 NH(CO)C₂H₅ cyclobutanyl 622 NH(CO)C₂H₅ cyclpentanyl 623 NH(CO)C₂H₅ cyclohexanyl 624 NH(CO)C₂H₅ cycloheptanyl 625 NH(CO)C₂H₅ phenyl 626 NH(CO)C₂H₅ phenylmethyl 627 NH(CO)C₂H₅ 3-hydroxyphenyl 628 NH(CO)C₂H₅ 3-hydroxy-4-methoxyphenyl 629 NH(CO)C₂H₅ 3-fluorophenyl 630 NH(CO)C₂H₅ 3-chlorophenyl 631 NH(CO)C₂H₅ 3-nitrophenyl 632 NH(CO)C₂H₅ 3-aminophenyl 633 NH(CO)C₂H₅ 3-methylsulfonamidephenyl 634 NH(CO)C₂H₅ 3-trifluoro- methylsulfonamidephenyl 635 NH(CO)C₂H₅ 3-Ac—NHphenyl 636 NH(CO)C₂H₅ 3-Boc—NHphenyl 637 NH(CO)C₂H₅ 3-Cbz—NHphenyl 638 NH(CO)C₂H₅ 3-aminomethylenephenyl 639 NH(CO)C₂H₅ 3-aminoethylenephenyl 640 NH(CO)C₂H₅ 3-cyanophenyl 641 NH(CO)C₂H₅ 3-cyanomethylphenyl 642 NH(CO)C₂H₅ 3-hydroxymethylenephenyl 643 NH(CO)C₂H₅ 3-carboxylphenyl 644 NH(CO)C₂H₅ 3-mercaptophenyl 645 NH(CO)C₂H₅ 3-methoxyphenyl 646 NH(CO)C₂H₅ 3,4-methylenedioxophenyl 647 NH(CO)C₂H₅ 3-tetrazolephenyl 648 NH(CO)C₂H₅ 3-aminosulfonylphenyl 649 NH(CO)C₂H₅ 3-methylamino- sulfonylphenyl 650 NH(CO)C₂H₅ 3-ethylamino-sulfonylphenyl 651 NH(CO)C₂H₅ 3-tert-butylamino- sulfonylphenyl 652 NH(CO)C₂H₅ 3-methylsulfonylphenyl 653 NH(CO)C₂H₅ 4-methoxyphenyl 654 NH(CO)C₂H₅ 4-phenylphenyl 655 NH(CO)C₂H₅ 4-(2-hydroxy- methylenephenyl)-phenyl 656 NH(CO)C₂H₅ 4-(2-tert-butylamino- sufonylphenyl)-phenyl 657 NH(CO)C₂H₅ 4-(2-methylamino- sufonylphenyl)-phenyl 658 NH(CO)C₂H₅ 4-(2-ethylamino- sufonylphenyl)-phenyl 659 NH(CO)C₂H₅ 4-(2-amino-sufonylphenyl)- phenyl 660 NH(CO)C₂H₅ 4-(2-chlorophenyl)-phenyl 661 NH(CO)C₂H₅ 4-(2-fluorophenyl)-phenyl 662 NH(CO)C₂H₅ 4-(2,4-dichlorophenyl)-phenyl 663 NH(CO)C₂H₅ 4-(2,6-dichlorophenyl)-phenyl 664 NH(CO)C₂H₅ 4-(3,5-dichlorophenyl)-phenyl 665 NH(CO)C₂H₅ 4-(2,3-dichlorophenyl)-phenyl 666 NH(CO)C₂H₅ 4-(2-methylphenyl)-phenyl 667 NH(CO)C₂H₅ 4-(2-tetrazole-phenyl)-phenyl 668 NH(CO)C₂H₅ 4-(2-methoxy-phenyl)-phenyl 669 NH(CO)C₂H₅ 4-(2-tmethyl-phenyl)-phenyl 670 NH(CO)C₂H₅ 4-(2-formyl-phenyl)-phenyl 671 NH(CO)C₂H₅ 4-(2-amino-phenyl)-phenyl 672 NH(CO)C₂H₅ 4-(2-methylamino-phenyl)- phenyl 673 NH(CO)C₂H₅ 4-(2-ethylamino-phenyl)- phenyl 674 NH(CO)C₂H₅ 4-(2-propylamino-phenyl)- phenyl 675 NH(CO)C₂H₅ 4-(2-methylsulfonylamino- phenyl)-phenyl 676 NH(CO)C₂H₅ 4-(2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 677 NH(CO)C₂H₅ 4-(3-methylphenyl)-phenyl 678 NH(CO)C₂H₅ 4-(3-isopropylphenyl)-phenyl 679 NH(CO)C₂H₅ 4-(3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 680 NH(CO)C₂H₅ 4-(3-methylsulfonylamino- phenyl)-phenyl 681 NH(CO)C₂H₅ 4-(3-amino-phenyl)-phenyl 682 NH(CO)C₂H₅ 4-(3-nitro-phenyl)-phenyl 683 NH(CO)C₂H₅ 2-pyridyl 684 NH(CO)C₂H₅ 3-pyridyl 685 NH(CO)C₂H₅ 4-pyridyl 686 NH(CO)C₂H₅ 3-amino-4-pyridyl 687 NH(CO)C₂H₅ 3-hydroxy-4-pyridyl 688 NH(CO)C₂H₅ 3-imidazole 689 NH(CO)C₂H₅ 2-nitro-3-imidazole 690 NH(CO)C₂H₅ 5-thiazole 691 NH(CO)C₂H₅ 5-oxazole 692 NH(CO)C₂H₅ 4-pyazole 693 NH(CO)C₂H₅ phenylethyl 694 NH(CO)C₂H₅ 2-aminophenylethyl 695 NH(CO)C₂H₅ 2-methylsulfonylamino- phenylethyl 696 NH(CO)C₂H₅ 2-trifluoromethylsulfonyl- amino-phenylethyl 697 NH(CO)C₂H₅ 2-hydroxymethylene- phenylethyl 698 NH(CO)C₂H₅ 2-aminomethylene- phenylethyl 699 NH(CO)C₂H₅ 2-tetrazolephenylethyl 700 NH(CO)C₂H₅ 2-tert-butylamino- sulfonylphenylethyl 701 NH(CO)C₂H₅ 2-aminosulfonyl-phenylethyl 702 NH(CO)C₂H₅ 2-methoxyphenylethyl 703 NH(CO)C₂H₅ 3-aminophenylethyl 704 NH(CO)C₂H₅ 3-methylsulfonylamino- phenylethyl 705 NH(CO)C₂H₅ 3-trifluoromethylsulfonyl- amino-phenylethyl 706 NH(CO)C₂H₅ 3-hydroxymethylene- phenylethyl 707 NH(CO)C₂H₅ 3-aminomethylene- phenylethyl 708 NH(CO)C₂H₅ 3-tetrazolephenylethyl 709 NH(CO)C₂H₅ 3-tert-butylamino- sulfonylphenylethyl 710 NH(CO)C₂H₅ 3-aminosulfonyl-phenylethyl 711 NH(CO)C₂H₅ 3-methoxyphenylethyl 712 NH(CO)OC₂H₅ H 713 NH(CO)OC₂H₅ methyl 714 NH(CO)OC₂H₅ ethyl 715 NH(CO)OC₂H₅ n-propyl 716 NH(CO)OC₂H₅ n-butyl 717 NH(CO)OC₂H₅ n-pentyl 718 NH(CO)OC₂H₅ n-hexanyl 719 NH(CO)OC₂H₅ n-heptanyl 720 NH(CO)OC₂H₅ isopropyl 721 NH(CO)OC₂H₅ tert-butyl 722 NH(CO)OC₂H₅ cyclopropyl 723 NH(CO)OC₂H₅ cyclobutanyl 724 NH(CO)OC₂H₅ cyclpentanyl 725 NH(CO)OC₂H₅ cyclohexanyl 726 NH(CO)OC₂H₅ cycloheptanyl 727 NH(CO)OC₂H₅ phenyl 728 NH(CO)OC₂H₅ phenylmethyl 729 NH(CO)OC₂H₅ 3-hydroxyphenyl 730 NH(CO)OC₂H₅ 3-hydroxy-4-methoxyphenyl 731 NH(CO)OC₂H₅ 3-fluorophenyl 732 NH(CO)OC₂H₅ 3-chlorophenyl 733 NH(CO)OC₂H₅ 3-nitrophenyl 734 NH(CO)OC₂H₅ 3-aminophenyl 735 NH(CO)OC₂H₅ 3-methyl-sulfonamidephenyl 736 NH(CO)OC₂H₅ 3-trifluoro- methylsulfonamidephenyl 737 NH(CO)OC₂H₅ 3-Ac—NHphenyl 738 NH(CO)OC₂H₅ 3-Boc—NHphenyl 739 NH(CO)OC₂H₅ 3-Cbz—NHphenyl 740 NH(CO)OC₂H₅ 3-aminomethylenephenyl 741 NH(CO)OC₂H₅ 3-aminoethylenephenyl 742 NH(CO)OC₂H₅ 3-cyanophenyl 743 NH(CO)OC₂H₅ 3-cyanomethylphenyl 744 NH(CO)OC₂H₅ 3-hydroxymethylenephenyl 745 NH(CO)OC₂H₅ 3-carboxylphenyl 746 NH(CO)OC₂H₅ 3-mercaptophenyl 747 NH(CO)OC₂H₅ 3-methoxyphenyl 748 NH(CO)OC₂H₅ 3,4-methylenedioxophenyl 749 NH(CO)OC₂H₅ 3-tetrazolephenyl 750 NH(CO)OC₂H₅ 3-aminosulfonylphenyl 751 NH(CO)OC₂H₅ 3-methylamino- sulfonylphenyl 752 NH(CO)OC₂H₅ 3-ethylamino-sulfonylphenyl 753 NH(CO)OC₂H₅ 3-tert-butylamino- sulfonylphenyl 754 NH(CO)OC₂H₅ 3-methylsulfonylphenyl 755 NH(CO)OC₂H₅ 4-methoxyphenyl 756 NH(CO)OC₂H₅ 4-phenylphenyl 757 NH(CO)OC₂H₅ 4-(2-hydroxy- methylenephenyl)-phenyl 758 NH(CO)OC₂H₅ 4-(2-tert-butylamino- sufonylphenyl)-phenyl 759 NH(CO)OC₂H₅ 4-(2-methylamino- sufonylphenyl)-phenyl 760 NH(CO)OC₂H₅ 4-(2-ethylamino- sufonylphenyl)-phenyl 761 NH(CO)OC₂H₅ 4-(2-aminosufonyl-phenyl)- phenyl 762 NH(CO)OC₂H₅ 4-(2-chlorophenyl)-phenyl 763 NH(CO)OC₂H₅ 4-(2-fluorophenyl)-phenyl 764 NH(CO)OC₂H₅ 4-(2,4-dichlorophenyl)-phenyl 765 NH(CO)OC₂H₅ 4-(2,6-dichlorophenyl)-phenyl 766 NH(CO)OC₂H₅ 4-(3,5-dichlorophenyl)-phenyl 767 NH(CO)OC₂H₅ 4-(2,3-dichlorophenyl)-phenyl 768 NH(CO)OC₂H₅ 4-(2-methylphenyl)-phenyl 769 NH(CO)OC₂H₅ 4-(2-tetrazole-phenyl)-phenyl 770 NH(CO)OC₂H₅ 4-(2-methoxy-phenyl)-phenyl 771 NH(CO)OC₂H₅ 4-(2-tmethyl-phenyl)-phenyl 772 NH(CO)OC₂H₅ 4-(2-formyl-phenyl)-phenyl 773 NH(CO)OC₂H₅ 4-(2-amino-phenyl)-phenyl 774 NH(CO)OC₂H₅ 4-(2-methylamino-phenyl)- phenyl 775 NH(CO)OC₂H₅ 4-(2-ethylamino-phenyl)- phenyl 776 NH(CO)OC₂H₅ 4-(2-propylamino-phenyl)- phenyl 777 NH(CO)OC₂H₅ 4-(2-methylsulfonylamino- phenyl)-phenyl 778 NH(CO)OC₂H₅ 4-(2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 779 NH(CO)OC₂H₅ 4-(3-methylphenyl)-phenyl 780 NH(CO)OC₂H₅ 4-(3-isopropylphenyl)-phenyl 781 NH(CO)OC₂H₅ 4-(3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 782 NH(CO)OC₂H₅ 4-(3-methylsulfonylamino- phenyl)-phenyl 783 NH(CO)OC₂H₅ 4-(3-amino-phenyl)-phenyl 784 NH(CO)OC₂H₅ 4-(3-nitro-phenyl)-phenyl 785 NH(CO)OC₂H₅ 2-pyridyl 786 NH(CO)OC₂H₅ 3-pyridyl 787 NH(CO)OC₂H₅ 4-pyridyl 788 NH(CO)OC₂H₅ 3-amino-4-pyridyl 789 NH(CO)OC₂H₅ 3-hydroxy-4-pyridyl 790 NH(CO)OC₂H₅ 3-imidazole 791 NH(CO)OC₂H₅ 2-nitro-3-imidazole 792 NH(CO)OC₂H₅ 5-thiazole 793 NH(CO)OC₂H₅ 5-oxazole 794 NH(CO)OC₂H₅ 4-pyazole 795 NH(CO)OC₂H₅ phenylethyl 796 NH(CO)OC₂H₅ 2-aminophenylethyl 797 NH(CO)OC₂H₅ 2-methylsulfonylamino- phenylethyl 798 NH(CO)OC₂H₅ 2-trifluoromethylsulfonyl- amino-phenylethyl 799 NH(CO)OC₂H₅ 2-hydroxymethylene- phenylethyl 800 NH(CO)OC₂H₅ 2-aminomethylene- phenylethyl 801 NH(CO)OC₂H₅ 2-tetrazolephenylethyl 802 NH(CO)OC₂H₅ 2-tert-butylamino- sulfonylphenylethyl 803 NH(CO)OC₂H₅ 2-aminosulfonyl-phenylethyl 804 NH(CO)OC₂H₅ 2-methoxyphenylethyl 805 NH(CO)OC₂H₅ 3-aminophenylethyl 806 NH(CO)OC₂H₅ 3-methylsulfonylamino- phenylethyl 807 NH(CO)OC₂H₅ 3-trifluoromethylsulfonyl- amino-phenylethyl 808 NH(CO)OC₂H₅ 3-hydroxymethylene- phenylethyl 809 NH(CO)OC₂H₅ 3-aminomethylene- phenylethyl 810 NH(CO)OC₂H₅ 3-tetrazolephenylethyl 811 NH(CO)OC₂H₅ 3-tert-butylamino- sulfonylphenylethyl 812 NH(CO)OC₂H₅ 3-aminosulfonyl-phenylethyl 813 NH(CO)OC₂H₅ 3-methoxyphenylethyl 814 NH(CO)OCH₃ H 815 NH(CO)OCH₃ methyl 816 NH(CO)OCH₃ ethyl 817 NH(CO)OCH₃ n-propyl 818 NH(CO)OCH₃ n-butyl 819 NH(CO)OCH₃ n-pentyl 820 NH(CO)OCH₃ n-hexanyl 821 NH(CO)OCH₃ n-heptanyl 822 NH(CO)OCH₃ isopropyl 823 NH(CO)OCH₃ tert-butyl 824 NH(CO)OCH₃ cyclopropyl 825 NH(CO)OCH₃ cyclobutanyl 826 NH(CO)OCH₃ cyclpentanyl 827 NH(CO)OCH₃ cyclohexanyl 828 NH(CO)OCH₃ cycloheptanyl 829 NH(CO)OCH₃ phenyl 830 NH(CO)OCH₃ phenylmethyl 831 NH(CO)OCH₃ 3-hydroxyphenyl 832 NH(CO)OCH₃ 3-hydroxy-4-methoxyphenyl 833 NH(CO)OCH₃ 3-fluorophenyl 834 NH(CO)OCH₃ 3-chlorophenyl 835 NH(CO)OCH₃ 3-nitrophenyl 836 NH(CO)OCH₃ 3-aminophenyl 837 NH(CO)OCH₃ 3-methyl-sulfonamidephenyl 838 NH(CO)OCH₃ 3-trifluoro- methylsulfonamidephenyl 839 NH(CO)OCH₃ 3-Ac—NHphenyl 840 NH(CO)OCH₃ 3-Boc—NHphenyl 841 NH(CO)OCH₃ 3-Cbz—NHphenyl 842 NH(CO)OCH₃ 3-aminomethylenephenyl 843 NH(CO)OCH₃ 3-aminoethylenephenyl 844 NH(CO)OCH₃ 3-cyanophenyl 845 NH(CO)OCH₃ 3-cyanomethylphenyl 846 NH(CO)OCH₃ 3-hydroxymethylenephenyl 847 NH(CO)OCH₃ 3-carboxylphenyl 848 NH(CO)OCH₃ 3-mercaptophenyl 849 NH(CO)OCH₃ 3-methoxyphenyl 850 NH(CO)OCH₃ 3,4-methylenedioxophenyl 851 NH(CO)OCH₃ 3-tetrazolephenyl 852 NH(CO)OCH₃ 3-aminosulfonylphenyl 853 NH(CO)OCH₃ 3-methylamino- sulfonylphenyl 854 NH(CO)OCH₃ 3-ethylamino-sulfonylphenyl 855 NH(CO)OCH₃ 3-tert-butylamino- sulfonylphenyl 856 NH(CO)OCH₃ 3-methylsulfonylphenyl 857 NH(CO)OCH₃ 4-methoxyphenyl 858 NH(CO)OCH₃ 4-phenylphenyl 859 NH(CO)OCH₃ 4-(2-hydroxy- methylenephenyl)-phenyl 860 NH(CO)OCH₃ 4-(2-tert-butylamino- sufonylphenyl)-phenyl 861 NH(CO)OCH₃ 4-(2-methylamino- sufonylphenyl)-phenyl 862 NH(CO)OCH₃ 4-(2-ethylamino- sufonylphenyl)-phenyl 863 NH(CO)OCH₃ 4-(2-aminosufonyl-phenyl)- phenyl 864 NH(CO)OCH₃ 4-(2-chlorophenyl)-phenyl 865 NH(CO)OCH₃ 4-(2-fluorophenyl)-phenyl 866 NH(CO)OCH₃ 4-(2,4-dichlorophenyl)-phenyl 867 NH(CO)OCH₃ 4-(2,6-dichlorophenyl)-phenyl 868 NH(CO)OCH₃ 4-(3,5-dichlorophenyl)-phenyl 869 NH(CO)OCH₃ 4-(2,3-dichlorophenyl)-phenyl 870 NH(CO)OCH₃ 4-(2-methylphenyl)-phenyl 871 NH(CO)OCH₃ 4-(2-tetrazole-phenyl)-phenyl 872 NH(CO)OCH₃ 4-(2-methoxy-phenyl)-phenyl 873 NH(CO)OCH₃ 4-(2-tmethyl-phenyl)-phenyl 874 NH(CO)OCH₃ 4-(2-formyl-phenyl)-phenyl 875 NH(CO)OCH₃ 4-(2-amino-phenyl)-phenyl 876 NH(CO)OCH₃ 4-(2-methylamino-phenyl)- phenyl 877 NH(CO)OCH₃ 4-(2-ethylamino-phenyl)- phenyl 878 NH(CO)OCH₃ 4-(2-propylamino-phenyl)- phenyl 879 NH(CO)OCH₃ 4-(2-methylsulfonylamino- phenyl)-phenyl 880 NH(CO)OCH₃ 4-(2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 881 NH(CO)OCH₃ 4-(3-methylphenyl)-phenyl 882 NH(CO)OCH₃ 4-(3-isopropylphenyl)-phenyl 883 NH(CO)OCH₃ 4-(3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 884 NH(CO)OCH₃ 4-(3-methylsulfonylamino- phenyl)-phenyl 885 NH(CO)OCH₃ 4-(3-amino-phenyl)-phenyl 886 NH(CO)OCH₃ 4-(3-nitro-phenyl)-phenyl 887 NH(CO)OCH₃ 2-pyridyl 888 NH(CO)OCH₃ 3-pyridyl 889 NH(CO)OCH₃ 4-pyridyl 890 NH(CO)OCH₃ 3-amino-4-pyridyl 891 NH(CO)OCH₃ 3-hydroxy-4-pyridyl 892 NH(CO)OCH₃ 3-imidazole 893 NH(CO)OCH₃ 2-nitro-3-imidazole 894 NH(CO)OCH₃ 5-thiazole 895 NH(CO)OCH₃ 5-oxazole 896 NH(CO)OCH₃ 4-pyazole 897 NH(CO)OCH₃ phenylethyl 898 NH(CO)OCH₃ 2-aminophenylethyl 899 NH(CO)OCH₃ 2-methylsulfonylamino- phenylethyl 900 NH(CO)OCH₃ 2-trifluoromethylsulfonyl- aminophenylethyl 901 NH(CO)OCH₃ 2-hydroxymethylene- phenylethyl 902 NH(CO)OCH₃ 2-aminomethylene- phenylethyl 903 NH(CO)OCH₃ 2-tetrazolephenylethyl 904 NH(CO)OCH₃ 2-tert-butylamino- sulfonylphenylethyl 905 NH(CO)OCH₃ 2-aminosulfonyl-phenylethyl 906 NH(CO)OCH₃ 2-methoxyphenylethyl 907 NH(CO)OCH₃ 3-aminophenylethyl 908 NH(CO)OCH₃ 3-methylsulfonylamino- phenylethyl 909 NH(CO)OCH₃ 3-trifluoromethylsulfonyl- amino-phenylethyl 910 NH(CO)OCH₃ 3-hydroxymethylene- phenylethyl 911 NH(CO)OCH₃ 3-aminomethylene- phenylethyl 912 NH(CO)OCH₃ 3-tetrazolephenylethyl 913 NH(CO)OCH₃ 3-tert-butylamino- sulfonylphenylethyl 914 NH(CO)OCH₃ 3-aminosulfonyl-phenylethyl 915 NH(CO)OCH₃ 3-methoxyphenylethyl 916 NHBoc H 917 NHBoc methyl 918 NHBoc ethyl 919 NHBoc n-propyl 920 NHBoc n-butyl 921 NHBoc n-pentyl 922 NHBoc n-hexanyl 923 NHBoc n-heptanyl 924 NHBoc isopropyl 925 NHBoc tert-butyl 926 NHBoc cyclopropyl 927 NHBoc cyclobutanyl 928 NHBoc cyclpentanyl 929 NHBoc cyclohexanyl 930 NHBoc cycloheptanyl 931 NHBoc phenyl 932 NHBoc phenylmethyl 933 NHBoc 3-hydroxyphenyl 934 NHBoc 3-hydroxy-4-methoxyphenyl 935 NHBoc 3-fluorophenyl 936 NHBoc 3-chlorophenyl 937 NHBoc 3-nitrophenyl 938 NHBoc 3-aminophenyl 939 NHBoc 3-methyl-sulfonamidephenyl 940 NHBoc 3-trifluoro- methylsulfonamidephenyl 941 NHBoc 3-Ac—NHphenyl 942 NHBoc 3-Boc—NHphenyl 943 NHBoc 3-Cbz—NHphenyl 944 NHBoc 3-aminomethylenephenyl 945 NHBoc 3-aminoethylenephenyl 946 NHBoc 3-cyanophenyl 947 NHBoc 3-cyanomethylphenyl 948 NHBoc 3-hydroxymethylenephenyl 949 NHBoc 3-carboxylphenyl 950 NHBoc 3-mercaptophenyl 951 NHBoc 3-methoxyphenyl 952 NHBoc 3,4-methylenedioxophenyl 953 NHBoc 3-tetrazolephenyl 954 NHBoc 3-aminosulfonylphenyl 955 NHBoc 3-methylamino- sulfonylphenyl 956 NHBoc 3-ethylamino-sulfonylphenyl 957 NHBoc 3-tert-butylamino- sulfonylphenyl 958 NHBoc 3-methylsulfonylphenyl 959 NHBoc 4-methoxyphenyl 960 NHBoc 4-phenylphenyl 961 NHBoc 4-(2-hydroxy- methylenephenyl)-phenyl 962 NHBoc 4-(2-tert-butylamino- sufonylphenyl)-phenyl 963 NHBoc 4-(2-methylamino- sufonylphenyl)-phenyl 964 NHBoc 4-(2-ethylamino- sufonylphenyl)-phenyl 965 NHBoc 4-(2-aminosufonyl-phenyl)- phenyl 966 NHBoc 4-(2-chlorophenyl)-phenyl 967 NHBoc 4-(2-fluorophenyl)-phenyl 968 NHBoc 4-(2,4-dichlorophenyl)-phenyl 969 NHBoc 4-(2,6-dichlorophenyl)-phenyl 970 NHBoc 4-(3,5-dichlorophenyl)-phenyl 971 NHBoc 4-(2,3-dichlorophenyl)-phenyl 972 NHBoc 4-(2-methylphenyl)-phenyl 973 NHBoc 4-(2-tetrazole-phenyl)-phenyl 974 NHBoc 4-(2-methoxy-phenyl)-phenyl 975 NHBoc 4-(2-tmethyl-phenyl)-phenyl 976 NHBoc 4-(2-formyl-phenyl)-phenyl 977 NHBoc 4-(2-amino-phenyl)-phenyl 978 NHBoc 4-(2-methylamino-phenyl)- phenyl 979 NHBoc 4-(2-ethylamino-phenyl)- phenyl 980 NHBoc 4-(2-propylamino-phenyl)- phenyl 981 NHBoc 4-(2-methylsulfonylamino- phenyl)-phenyl 982 NHBoc 4-(2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 983 NHBoc 4-(3-methylphenyl)-phenyl 984 NHBoc 4-(3-isopropylphenyl)-phenyl 985 NHBoc 4-(3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 986 NHBoc 4-(3-methylsulfonylamino- phenyl)-phenyl 987 NHBoc 4-(3-amino-phenyl)-phenyl 988 NHBoc 4-(3-nitro-phenyl)-phenyl 989 NHBoc 2-pyridyl 990 NHBoc 3-pyridyl 991 NHBoc 4-pyridyl 992 NHBoc 3-amino-4-pyridyl 993 NHBoc 3-hydroxy-4-pyridyl 994 NHBoc 3-imidazole 995 NHBoc 2-nitro-3-imidazole 996 NHBoc 5-thiazole 997 NHBoc 5-oxazole 998 NHBoc 4-pyazole 999 NHBoc phenylethyl 1000 NHBoc 2-aminophenylethyl 1001 NHBoc 2-methylsulfonylamino- phenylethyl 1002 NHBoc 2-trifluoromethylsulfonyl- amino-phenylethyl 1003 NHBoc 2-hydroxymethylene- phenylethyl 1004 NHBoc 2-aminomethylene- phenylethyl 1005 NHBoc 2-tetrazolephenylethyl 1006 NHBoc 2-tert-butylamino- sulfonylphenylethyl 1007 NHBoc 2-aminosulfonyl-phenylethyl 1008 NHBoc 2-methoxyphenylethyl 1009 NHBoc 3-aminophenylethyl 1010 NHBoc 3-methylsulfonylamino- phenylethyl 1011 NHBoc 3-trifluoromethylsulfonyl- amino-phenylethyl 1012 NHBoc 3-hydroxymethylene- phenylethyl 1013 NHBoc 3-aminomethylene- phenylethyl 1014 NHBoc 3-tetrazolephenylethyl 1015 NHBoc 3-tert-butylamino- sulfonylphenylethyl 1016 NHBoc 3-aminosulfonyl-phenylethyl 1017 NHBoc 3-methoxyphenylethyl 1018 NH(CO)OCH₂-4-pyridyl H 1019 NH(CO)OCH₂-4-pyridyl methyl 1020 NH(CO)OCH₂-4-pyridyl ethyl 1021 NH(CO)OCH₂-4-pyridyl n-propyl 1022 NH(CO)OCH₂-4-pyridyl n-butyl 1023 NH(CO)OCH₂-4-pyridyl n-pentyl 1024 NH(CO)OCH₂-4-pyridyl n-hexanyl 1025 NH(CO)OCH₂-4-pyridyl n-heptanyl 1026 NH(CO)OCH₂-4-pyridyl isopropyl 1027 NH(CO)OCH₂-4-pyridyl tert-butyl 1028 NH(CO)OCH₂-4-pyridyl cyclopropyl 1029 NH(CO)OCH₂-4-pyridyl cyclobutanyl 1030 NH(CO)OCH₂-4-pyridyl cyclpentanyl 1031 NH(CO)OCH₂-4-pyridyl cyclohexanyl 1032 NH(CO)OCH₂-4-pyridyl cycloheptanyl 1033 NH(CO)OCH₂-4-pyridyl phenyl 1034 NH(CO)OCH₂-4-pyridyl phenylmethyl 1035 NH(CO)OCH₂-4-pyridyl 3-hydroxyphenyl 1036 NH(CO)OCH₂-4-pyridyl 3-hydroxy-4-methoxyphenyl 1037 NH(CO)OCH₂-4-pyridyl 3-fluorophenyl 1038 NH(CO)OCH₂-4-pyridyl 3-chlorophenyl 1039 NH(CO)OCH₂-4-pyridyl 3-nitrophenyl 1040 NH(CO)OCH₂-4-pyridyl 3-aminophenyl 1041 NH(CO)OCH₂-4-pyridyl 3-methyl-sulfonamidephenyl 1042 NH(CO)OCH₂-4-pyridyl 3-trifluoro- methylsulfonamidephenyl 1043 NH(CO)OCH₂-4-pyridyl 3-Ac—NHphenyl 1044 NH(CO)OCH₂-4-pyridyl 3-Boc—NHphenyl 1045 NH(CO)OCH₂-4-pyridyl 3-Cbz—NHphenyl 1046 NH(CO)OCH₂-4-pyridyl 3-aminomethylenephenyl 1047 NH(CO)OCH₂-4-pyridyl 3-aminoethylenephenyl 1048 NH(CO)OCH₂-4-pyridyl 3-cyanophenyl 1049 NH(CO)OCH₂-4-pyridyl 3-cyanomethylphenyl 1050 NH(CO)OCH₂-4-pyridyl 3-hydroxymethylenephenyl 1051 NH(CO)OCH₂-4-pyridyl 3-carboxylphenyl 1052 NH(CO)OCH₂-4-pyridyl 3-mercaptophenyl 1053 NH(CO)OCH₂-4-pyridyl 3-methoxyphenyl 1054 NH(CO)OCH₂-4-pyridyl 3,4-methylenedioxophenyl 1055 NH(CO)OCH₂-4-pyridyl 3-tetrazolephenyl 1056 NH(CO)OCH₂-4-pyridyl 3-aminosulfonylphenyl 1057 NH(CO)OCH₂-4-pyridyl 3-methylamino- sulfonylphenyl 1058 NH(CO)OCH₂-4-pyridyl 3-ethylamino-sulfonylphenyl 1059 NH(CO)OCH₂-4-pyridyl 3-tert-butylamino- sulfonylphenyl 1060 NH(CO)OCH₂-4-pyridyl 3-methylsulfonylphenyl 1061 NH(CO)OCH₂-4-pyridyl 4-methoxyphenyl 1062 NH(CO)OCH₂-4-pyridyl 4-phenylphenyl 1063 NH(CO)OCH₂-4-pyridyl 4-(2-hydroxy- methylenephenyl)-phenyl 1064 NH(CO)OCH₂-4-pyridyl 4-(2-tert-butylamino- sufonylphenyl)-phenyl 1065 NH(CO)OCH₂-4-pyridyl 4-(2-methylamino- sufonylphenyl)-phenyl 1066 NH(CO)OCH₂-4-pyridyl 4-(2-ethylamino- sufonylphenyl)-phenyl 1067 NH(CO)OCH₂-4-pyridyl 4-(2-aminosufonyl-phenyl)- phenyl 1068 NH(CO)OCH₂-4-pyridyl 4-(2-chlorophenyl)-phenyl 1069 NH(CO)OCH₂-4-pyridyl 4-(2-fluorophenyl)-phenyl 1070 NH(CO)OCH₂-4-pyridyl 4-(2,4-dichlorophenyl)-phenyl 1071 NH(CO)OCH₂-4-pyridyl 4-(2,6-dichlorophenyl)-phenyl 1072 NH(CO)OCH₂-4-pyridyl 4-(3,5-dichlorophenyl)-phenyl 1073 NH(CO)OCH₂-4-pyridyl 4-(2,3-dichlorophenyl)-phenyl 1074 NH(CO)OCH₂-4-pyridyl 4-(2-methylphenyl)-phenyl 1075 NH(CO)OCH₂-4-pyridyl 4-(2-tetrazole-phenyl)-phenyl 1076 NH(CO)OCH₂-4-pyridyl 4-(2-methoxy-phenyl)-phenyl 1077 NH(CO)OCH₂-4-pyridyl 4-(2-tmethyl-phenyl)-phenyl 1078 NH(CO)OCH₂-4-pyridyl 4-(2-formyl-phenyl)-phenyl 1079 NH(CO)OCH₂-4-pyridyl 4-(2-amino-phenyl)-phenyl 1080 NH(CO)OCH₂-4-pyridyl 4-(2-methylamino-phenyl)- phenyl 1081 NH(CO)OCH₂-4-pyridyl 4-(2-ethylamino-phenyl)- phenyl 1082 NH(CO)OCH₂-4-pyridyl 4-(2-propylamino-phenyl)- phenyl 1083 NH(CO)OCH₂-4-pyridyl 4-(2-methylsulfonylamino- phenyl)-phenyl 1084 NH(CO)OCH₂-4-pyridyl 4-(2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1085 NH(CO)OCH₂-4-pyridyl 4-(3-methylphenyl)-phenyl 1086 NH(CO)OCH₂-4-pyridyl 4-(3-isopropylphenyl)-phenyl 1087 NH(CO)OCH₂-4-pyridyl 4-(3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1088 NH(CO)OCH₂-4-pyridyl 4-(3-methylsulfonylamino- phenyl)-phenyl 1089 NH(CO)OCH₂-4-pyridyl 4-(3-amino-phenyl)-phenyl 1090 NH(CO)OCH₂-4-pyridyl 4-(3-nitro-phenyl)-phenyl 1091 NH(CO)OCH₂-4-pyridyl 2-pyridyl 1092 NH(CO)OCH₂-4-pyridyl 3-pyridyl 1093 NH(CO)OCH₂-4-pyridyl 4-pyridyl 1094 NH(CO)OCH₂-4-pyridyl 3-amino-4-pyridyl 1095 NH(CO)OCH₂-4-pyridyl 3-hydroxy-4-pyridyl 1096 NH(CO)OCH₂-4-pyridyl 3-imidazole 1097 NH(CO)OCH₂-4-pyridyl 2-nitro-3-imidazole 1098 NH(CO)OCH₂-4-pyridyl 5-thiazole 1099 NH(CO)OCH₂-4-pyridyl 5-oxazole 1100 NH(CO)OCH₂-4-pyridyl 4-pyazole 1101 NH(CO)OCH₂-4-pyridyl phenylethyl 1102 NH(CO)OCH₂-4-pyridyl 2-aminophenylethyl 1103 NH(CO)OCH₂-4-pyridyl 2-methylsulfonylamino- phenylethyl 1104 NH(CO)OCH₂-4-pyridyl 2-trifluoromethylsulfonyl- amino-phenylethyl 1105 NH(CO)OCH₂-4-pyridyl 2-hydroxymethylene- phenylethyl 1106 NH(CO)OCH₂-4-pyridyl 2-aminomethylene- phenylethyl 1107 NH(CO)OCH₂-4-pyridyl 2-tetrazolephenylethyl 1108 NH(CO)OCH₂-4-pyridyl 2-tert-butylamino- sulfonylphenylethyl 1109 NH(CO)OCH₂-4-pyridyl 2-aminosulfonyl-phenylethyl 1110 NH(CO)OCH₂-4-pyridyl 2-methoxyphenylethyl 1111 NH(CO)OCH₂-4-pyridyl 3-aminophenylethyl 1112 NH(CO)OCH₂-4-pyridyl 3-methylsulfonylamino- phenylethyl 1113 NH(CO)OCH₂-4-pyridyl 3-trifluoromethylsulfonyl- amino-phenylethyl 1114 NH(CO)OCH₂-4-pyridyl 3-hydroxymethylene- phenylethyl 1115 NH(CO)OCH₂-4-pyridyl 3-aminomethylene- phenylethyl 1116 NH(CO)OCH₂-4-pyridyl 3-tetrazolephenylethyl 1117 NH(CO)OCH₂-4-pyridyl 3-tert-butylamino- sulfonylphenylethyl 1118 NH(CO)OCH₂-4-pyridyl 3-aminosulfonyl-phenylethyl 1119 NH(CO)OCH₂-4-pyridyl 3-methoxyphenylethyl 1120 NHS(O₂)CH₃ H 1121 NHS(O₂)CH₃ methyl 1122 NHS(O₂)CH₃ ethyl 1123 NHS(O₂)CH₃ n-propyl 1124 NHS(O₂)CH₃ n-butyl 1125 NHS(O₂)CH₃ n-pentyl 1126 NHS(O₂)CH₃ n-hexanyl 1127 NHS(O₂)CH₃ n-heptanyl 1128 NHS(O₂)CH₃ isopropyl 1129 NHS(O₂)CH₃ tert-butyl 1130 NHS(O₂)CH₃ cyclopropyl 1131 NHS(O₂)CH₃ cyclobutanyl 1132 NHS(O₂)CH₃ cyclpentanyl 1133 NHS(O₂)CH₃ cyclohexanyl 1134 NHS(O₂)CH₃ cycloheptanyl 1135 NHS(O₂)CH₃ phenyl 1136 NHS(O₂)CH₃ phenylmethyl 1137 NHS(O₂)CH₃ 3-hydroxyphenyl 1138 NHS(O₂)CH₃ 3-hydroxy-4-methoxyphenyl 1139 NHS(O₂)CH₃ 3-fluorophenyl 1140 NHS(O₂)CH₃ 3-chlorophenyl 1141 NHS(O₂)CH₃ 3-nitrophenyl 1142 NHS(O₂)CH₃ 3-aminophenyl 1143 NHS(O₂)CH₃ 3-methyl-sulfonamidephenyl 1144 NHS(O₂)CH₃ 3-trifluoro- methylsulfonamidephenyl 1145 NHS(O₂)CH₃ 3-Ac—NHphenyl 1146 NHS(O₂)CH₃ 3-Boc—NHphenyl 1147 NHS(O₂)CH₃ 3-Cbz—NHphenyl 1148 NHS(O₂)CH₃ 3-aminomethylenephenyl 1149 NHS(O₂)CH₃ 3-aminoethylenephenyl 1150 NHS(O₂)CH₃ 3-cyanophenyl 1151 NHS(O₂)CH₃ 3-cyanomethylphenyl 1152 NHS(O₂)CH₃ 3-hydroxymethylenephenyl 1153 NHS(O₂)CH₃ 3-carboxylphenyl 1154 NHS(O₂)CH₃ 3-mercaptophenyl 1155 NHS(O₂)CH₃ 3-methoxyphenyl 1156 NHS(O₂)CH₃ 3,4-methylenedioxophenyl 1157 NHS(O₂)CH₃ 3-tetrazolephenyl 1158 NHS(O₂)CH₃ 3-aminosulfonylphenyl 1159 NHS(O₂)CH₃ 3-methylamino- sulfonylphenyl 1160 NHS(O₂)CH₃ 3-ethylamino-sulfonylphenyl 1161 NHS(O₂)CH₃ 3-tert-butylamino- sulfonylphenyl 1162 NHS(O₂)CH₃ 3-methylsulfonylphenyl 1163 NHS(O₂)CH₃ 4-methoxyphenyl 1164 NHS(O₂)CH₃ 4-phenylphenyl 1165 NHS(O₂)CH₃ 4-(2-hydroxy- methylenephenyl)-phenyl 1166 NHS(O₂)CH₃ 4-(2-tert-butylamino- sufonylphenyl)-phenyl 1167 NHS(O₂)CH₃ 4-(2-methylamino- sufonylphenyl)-phenyl 1168 NHS(O₂)CH₃ 4-(2-ethylamino- sufonylphenyl)-phenyl 1169 NHS(O₂)CH₃ 4-(2-aminosufonyl-phenyl)- phenyl 1170 NHS(O₂)CH₃ 4-(2-chlorophenyl)-phenyl 1171 NHS(O₂)CH₃ 4-(2-fluorophenyl)-phenyl 1172 NHS(O₂)CH₃ 4-(2,4-dichlorophenyl)-phenyl 1173 NHS(O₂)CH₃ 4-(2,6-dichlorophenyl)-phenyl 1174 NHS(O₂)CH₃ 4-(3,5-dichlorophenyl)-phenyl 1175 NHS(O₂)CH₃ 4-(2,3-dichlorophenyl)-phenyl 1176 NHS(O₂)CH₃ 4-(2-methylphenyl)-phenyl 1177 NHS(O₂)CH₃ 4-(2-tetrazole-phenyl)-phenyl 1178 NHS(O₂)CH₃ 4-(2-methoxy-phenyl)-phenyl 1179 NHS(O₂)CH₃ 4-(2-tmethyl-phenyl)-phenyl 1180 NHS(O₂)CH₃ 4-(2-formyl-phenyl)-phenyl 1181 NHS(O₂)CH₃ 4-(2-amino-phenyl)-phenyl 1182 NHS(O₂)CH₃ 4-(2-methylamino-phenyl)- phenyl 1183 NHS(O₂)CH₃ 4-(2-ethylamino-phenyl)- phenyl 1184 NHS(O₂)CH₃ 4-(2-propylamino-phenyl)- phenyl 1185 NHS(O₂)CH₃ 4-(2-methylsulfonylamino- phenyl)-phenyl 1186 NHS(O₂)CH₃ 4-(2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1187 NHS(O₂)CH₃ 4-(3-methylphenyl)-phenyl 1188 NHS(O₂)CH₃ 4-(3-isopropylphenyl)-phenyl 1189 NHS(O₂)CH₃ 4-(3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1190 NHS(O₂)CH₃ 4-(3-methylsulfonylamino- phenyl)-phenyl 1191 NHS(O₂)CH₃ 4-(3-amino-phenyl)-phenyl 1192 NHS(O₂)CH₃ 4-(3-nitro-phenyl)-phenyl 1193 NHS(O₂)CH₃ 2-pyridyl 1194 NHS(O₂)CH₃ 3-pyridyl 1195 NHS(O₂)CH₃ 4-pyridyl 1196 NHS(O₂)CH₃ 3-amino-4-pyridyl 1197 NHS(O₂)CH₃ 3-hydroxy-4-pyridyl 1198 NHS(O₂)CH₃ 3-imidazole 1199 NHS(O₂)CH₃ 2-nitro-3-imidazole 1200 NHS(O₂)CH₃ 5-thiazole 1201 NHS(O₂)CH₃ 5-oxazole 1202 NHS(O₂)CH₃ 4-pyazole 1203 NHS(O₂)CH₃ phenylethyl 1204 NHS(O₂)CH₃ 2-aminophenylethyl 1205 NHS(O₂)CH₃ 2-methylsulfonylamino- phenylethyl 1206 NHS(O₂)CH₃ 2-trifluoromethylsulfonyl- amino-phenylethyl 1207 NHS(O₂)CH₃ 2-hydroxymethylene- phenylethyl 1208 NHS(O₂)CH₃ 2-aminomethylene- phenylethyl 1209 NHS(O₂)CH₃ 2-tetrazolephenylethyl 1210 NHS(O₂)CH₃ 2-tert-butylamino- sulfonylphenylethyl 1211 NHS(O₂)CH₃ 2-aminosulfonyl-phenylethyl 1212 NHS(O₂)CH₃ 2-methoxyphenylethyl 1213 NHS(O₂)CH₃ 3-aminophenylethyl 1214 NHS(O₂)CH₃ 3-methylsulfonylamino- phenylethyl 1215 NHS(O₂)CH₃ 3-trifluoromethylsulfonyl- amino-phenylethyl 1216 NHS(O₂)CH₃ 3-hydroxymethylene- phenylethyl 1217 NHS(O₂)CH₃ 3-aminomethylene- phenylethyl 1218 NHS(O₂)CH₃ 3-tetrazolephenylethyl 1219 NHS(O₂)CH₃ 3-tert-butylamino- sulfonylphenylethyl 1220 NHS(O₂)CH₃ 3-aminosulfonyl-phenylethyl 1221 NHS(O₂)CH₃ 3-methoxyphenylethyl 1222 NHS(O₂)CF₃ H 1223 NHS(O₂)CF₃ methyl 1224 NHS(O₂)CF₃ ethyl 1225 NHS(O₂)CF₃ n-propyl 1226 NHS(O₂)CF₃ n-butyl 1227 NHS(O₂)CF₃ n-pentyl 1228 NHS(O₂)CF₃ n-hexanyl 1229 NHS(O₂)CF₃ n-heptanyl 1230 NHS(O₂)CF₃ isopropyl 1231 NHS(O₂)CF₃ tert-butyl 1232 NHS(O₂)CF₃ cyclopropyl 1233 NHS(O₂)CF₃ cyclobutanyl 1234 NHS(O₂)CF₃ cyclpentanyl 1235 NHS(O₂)CF₃ cyclohexanyl 1236 NHS(O₂)CF₃ cycloheptanyl 1237 NHS(O₂)CF₃ phenyl 1238 NHS(O₂)CF₃ phenylmethyl 1239 NHS(O₂)CF₃ 3-hydroxyphenyl 1240 NHS(O₂)CF₃ 3-hydroxy-4-methoxyphenyl 1241 NHS(O₂)CF₃ 3-fluorophenyl 1242 NHS(O₂)CF₃ 3-chlorophenyl 1243 NHS(O₂)CF₃ 3-nitrophenyl 1244 NHS(O₂)CF₃ 3-aminophenyl 1245 NHS(O₂)CF₃ 3-methyl-sulfonamidephenyl 1246 NHS(O₂)CF₃ 3-trifluoro- methylsulfonamidephenyl 1247 NHS(O₂)CF₃ 3-Ac—NHphenyl 1248 NHS(O₂)CF₃ 3-Boc—NHphenyl 1249 NHS(O₂)CF₃ 3-Cbz—NHphenyl 1250 NHS(O₂)CF₃ 3-aminomethylenephenyl 1251 NHS(O₂)CF₃ 3-aminoethylenephenyl 1252 NHS(O₂)CF₃ 3-cyanophenyl 1253 NHS(O₂)CF₃ 3-cyanomethylphenyl 1254 NHS(O₂)CF₃ 3-hydroxymethylenephenyl 1255 NHS(O₂)CF₃ 3-carboxylphenyl 1256 NHS(O₂)CF₃ 3-mercaptophenyl 1257 NHS(O₂)CF₃ 3-methoxyphenyl 1258 NHS(O₂)CF₃ 3,4-methylenedioxophenyl 1259 NHS(O₂)CF₃ 3-tetrazolephenyl 1260 NHS(O₂)CF₃ 3-aminosulfonylphenyl 1261 NHS(O₂)CF₃ 3-methylamino- sulfonylphenyl 1262 NHS(O₂)CF₃ 3-ethylamino-sulfonylphenyl 1263 NHS(O₂)CF₃ 3-tert-butylamino- sulfonylphenyl 1264 NHS(O₂)CF₃ 3-methylsulfonylphenyl 1265 NHS(O₂)CF₃ 4-methoxyphenyl 1266 NHS(O₂)CF₃ 4-phenylphenyl 1267 NHS(O₂)CF₃ 4-(2-hydroxy- methylenephenyl)-phenyl 1268 NHS(O₂)CF₃ 4-(2-tert-butylamino- sufonylphenyl)-phenyl 1269 NHS(O₂)CF₃ 4-(2-methylamino- sufonylphenyl)-phenyl 1270 NHS(O₂)CF₃ 4-(2-ethylamino- sufonylphenyl)-phenyl 1271 NHS(O₂)CF₃ 4-(2-aminosufonyl-phenyl)- phenyl 1272 NHS(O₂)CF₃ 4-(2-chlorophenyl)-phenyl 1273 NHS(O₂)CF₃ 4-(2-fluorophenyl)-phenyl 1274 NHS(O₂)CF₃ 4-(2,4-dichlorophenyl)-phenyl 1275 NHS(O₂)CF₃ 4-(2,6-dichlorophenyl)-phenyl 1276 NHS(O₂)CF₃ 4-(3,5-dichlorophenyl)-phenyl 1277 NHS(O₂)CF₃ 4-(2,3-dichlorophenyl)-phenyl 1278 NHS(O₂)CF₃ 4-(2-methylphenyl)-phenyl 1279 NHS(O₂)CF₃ 4-(2-tetrazole-phenyl)-phenyl 1280 NHS(O₂)CF₃ 4-(2-methoxy-phenyl)-phenyl 1281 NHS(O₂)CF₃ 4-(2-tmethyl-phenyl)-phenyl 1282 NHS(O₂)CF₃ 4-(2-formyl-phenyl)-phenyl 1283 NHS(O₂)CF₃ 4-(2-amino-phenyl)-phenyl 1284 NHS(O₂)CF₃ 4-(2-methylamino-phenyl)- phenyl 1285 NHS(O₂)CF₃ 4-(2-ethylamino-phenyl)- phenyl 1286 NHS(O₂)CF₃ 4-(2-propylamino-phenyl)- phenyl 1287 NHS(O₂)CF₃ 4-(2-methylsulfonylamino- phenyl)-phenyl 1288 NHS(O₂)CF₃ 4-(2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1289 NHS(O₂)CF₃ 4-(3-methylphenyl)-phenyl 1290 NHS(O₂)CF₃ 4-(3-isopropylphenyl)-phenyl 1291 NHS(O₂)CF₃ 4-(3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1292 NHS(O₂)CF₃ 4-(3-methylsulfonylamino- phenyl)-phenyl 1293 NHS(O₂)CF₃ 4-(3-amino-phenyl)-phenyl 1294 NHS(O₂)CF₃ 4-(3-nitro-phenyl)-phenyl 1295 NHS(O₂)CF₃ 2-pyridyl 1296 NHS(O₂)CF₃ 3-pyridyl 1297 NHS(O₂)CF₃ 4-pyridyl 1298 NHS(O₂)CF₃ 3-amino-4-pyridyl 1299 NHS(O₂)CF₃ 3-hydroxy-4-pyridyl 1300 NHS(O₂)CF₃ 3-imidazole 1301 NHS(O₂)CF₃ 2-nitro-3-imidazole 1302 NHS(O₂)CF₃ 5-thiazole 1303 NHS(O₂)CF₃ 5-oxazole 1304 NHS(O₂)CF₃ 4-pyazole 1305 NHS(O₂)CF₃ phenylethyl 1306 NHS(O₂)CF₃ 2-aminophenylethyl 1307 NHS(O₂)CF₃ 2-methylsulfonylamino- phenylethyl 1308 NHS(O₂)CF₃ 2-trifluoromethylsulfonyl- amino-phenylethyl 1309 NHS(O₂)CF₃ 2-hydroxymethylene- phenylethyl 1310 NHS(O₂)CF₃ 2-aminomethylene- phenylethyl 1311 NHS(O₂)CF₃ 2-tetrazolephenylethyl 1312 NHS(O₂)CF₃ 2-tert-butylamino- sulfonylphenylethyl 1313 NHS(O₂)CF₃ 2-aminosulfonyl-phenylethyl 1314 NHS(O₂)CF₃ 2-methoxyphenylethyl 1315 NHS(O₂)CF₃ 3-aminophenylethyl 1316 NHS(O₂)CF₃ 3-methylsulfonylamino- phenylethyl 1317 NHS(O₂)CF₃ 3-trifluoromethylsulfonyl- amino-phenylethyl 1318 NHS(O₂)CF₃ 3-hydroxymethylene- phenylethyl 1319 NHS(O₂)CF₃ 3-aminomethylene- phenylethyl 1320 NHS(O₂)CF₃ 3-tetrazolephenylethyl 1321 NHS(O₂)CF₃ 3-tert-butylamino- sulfonylphenylethyl 1322 NHS(O₂)CF₃ 3-aminosulfonyl-phenylethyl 1323 NHS(O₂)CF₃ 3-methoxyphenylethyl 1324 4-aminophenylS(O)2NH H 1325 4-aminophenylS(O)2NH methyl 1326 4-aminophenylS(O)2NH ethyl 1327 4-aminophenylS(O)2NH n-propyl 1328 4-aminophenylS(O)2NH n-butyl 1329 4-aminophenylS(O)2NH n-pentyl 1330 4-aminophenylS(O)2NH n-hexanyl 1331 4-aminophenylS(O)2NH n-heptanyl 1332 4-aminophenylS(O)2NH isopropyl 1333 4-aminophenylS(O)2NH tert-butyl 1334 4-aminophenylS(O)2NH cyclopropyl 1335 4-aminophenylS(O)2NH cyclobutanyl 1336 4-aminophenylS(O)2NH cyclpentanyl 1337 4-aminophenylS(O)2NH cyclohexanyl 1338 4-aminophenylS(O)2NH cycloheptanyl 1339 4-aminophenylS(O)2NH phenyl 1340 4-aminophenylS(O)2NH phenylmethyl 1341 4-aminophenylS(O)2NH 3-hydroxyphenyl 1342 4-aminophenylS(O)2NH 3-hydroxy-4-methoxyphenyl 1343 4-aminophenylS(O)2NH 3-fluorophenyl 1344 4-aminophenylS(O)2NH 3-chlorophenyl 1345 4-aminophenylS(O)2NH 3-nitrophenyl 1346 4-aminophenylS(O)2NH 3-aminophenyl 1347 4-aminophenylS(O)2NH 3-methyl-sulfonamidephenyl 1348 4-aminophenylS(O)2NH 3-trifluoro- methylsulfonamidephenyl 1349 4-aminophenylS(O)2NH 3-Ac—NHphenyl 1350 4-aminophenylS(O)2NH 3-Boc—NHphenyl 1351 4-aminophenylS(O)2NH 3-Cbz—NHphenyl 1352 4-aminophenylS(O)2NH 3-aminomethylenephenyl 1353 4-aminophenylS(O)2NH 3-aminoethylenephenyl 1354 4-aminophenylS(O)2NH 3-cyanophenyl 1355 4-aminophenylS(O)2NH 3-cyanomethylphenyl 1356 4-aminophenylS(O)2NH 3-hydroxymethylenephenyl 1357 4-aminophenylS(O)2NH 3-carboxylphenyl 1358 4-aminophenylS(O)2NH 3-mercaptophenyl 1359 4-aminophenylS(O)2NH 3-methoxyphenyl 1360 4-aminophenylS(O)2NH 3,4-methylenedioxophenyl 1361 4-aminophenylS(O)2NH 3-tetrazolephenyl 1362 4-aminophenylS(O)2NH 3-aminosulfonylphenyl 1363 4-aminophenylS(O)2NH 3-methylamino- sulfonylphenyl 1364 4-aminophenylS(O)2NH 3-ethylamino-sulfonylphenyl 1365 4-aminophenylS(O)2NH 3-tert-butylamino- sulfonylphenyl 1366 4-aminophenylS(O)2NH 3-methylsulfonylphenyl 1367 4-aminophenylS(O)2NH 4-methoxyphenyl 1368 4-aminophenylS(O)2NH 4-phenylphenyl 1369 4-aminophenylS(O)2NH 4-(2-hydroxy- methylenephenyl)-phenyl 1370 4-aminophenylS(O)2NH 4-(2-tert-butylamino- sufonylphenyl)-phenyl 1371 4-aminophenylS(O)2NH 4-(2-methylamino- sufonylphenyl)-phenyl 1372 4-aminophenylS(O)2NH 4-(2-ethylamino- sufonylphenyl)-phenyl 1373 4-aminophenylS(O)2NH 4-(2-aminosufonyl-phenyl)- phenyl 1374 4-aminophenylS(O)2NH 4-(2-chlorophenyl)-phenyl 1375 4-aminophenylS(O)2NH 4-(2-fluorophenyl)-phenyl 1376 4-aminophenylS(O)2NH 4-(2,4-dichlorophenyl)-phenyl 1377 4-aminophenylS(O)2NH 4-(2,6-dichlorophenyl)-phenyl 1378 4-aminophenylS(O)₂NH 4-(3,5-dichlorophenyl)-phenyl 1379 4-aminophenylS(O)₂NH 4-(2,3-dichlorophenyl)-phenyl 1380 4-aminophenylS(O)₂NH 4-(2-methylphenyl)-phenyl 1381 4-aminophenylS(O)₂NH 4-(2-tetrazole-phenyl)-phenyl 1382 4-aminophenylS(O)₂NH 4-(2-methoxy-phenyl)-phenyl 1383 4-aminophenylS(O)₂NH 4-(2-tmethyl-phenyl)-phenyl 1384 4-aminophenylS(O)₂NH 4-(2-formyl-phenyl)-phenyl 1385 4-aminophenylS(O)₂NH 4-(2-amino-phenyl)-phenyl 1386 4-aminophenylS(O)₂NH 4-(2-methylamino-phenyl)- phenyl 1387 4-aminophenylS(O)₂NH 4-(2-ethylamino-phenyl)- phenyl 1388 4-aminophenylS(O)₂NH 4-(2-propylamino-phenyl)- phenyl 1389 4-aminophenylS(O)₂NH 4-(2-methylsulfonylamino- phenyl)-phenyl 1390 4-aminophenylS(O)₂NH 4-(2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1391 4-aminophenylS(O)₂NH 4-(3-methylphenyl)-phenyl 1392 4-aminophenylS(O)₂NH 4-(3-isopropylphenyl)-phenyl 1393 4-aminophenylS(O)₂NH 4-(3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1394 4-aminophenylS(O)₂NH 4-(3-methylsulfonylamino- phenyl)-phenyl 1395 4-aminophenylS(O)₂NH 4-(3-amino-phenyl)-phenyl 1396 4-aminophenylS(O)₂NH 4-(3-nitro-phenyl)-phenyl 1397 4-aminophenylS(O)₂NH 2-pyridyl 1398 4-aminophenylS(O)₂NH 3-pyridyl 1399 4-aminophenylS(O)₂NH 4-pyridyl 1400 4-aminophenylS(O)₂NH 3-amino-4-pyridyl 1401 4-aminophenylS(O)₂NH 3-hydroxy-4-pyridyl 1402 4-aminophenylS(O)₂NH 3-imidazole 1403 4-aminophenylS(O)₂NH 2-nitro-3-imidazole 1404 4-aminophenylS(O)₂NH 5-thiazole 1405 4-aminophenylS(O)₂NH 5-oxazole 1406 4-aminophenylS(O)₂NH 4-pyazole 1407 4-aminophenylS(O)₂NH phenylethyl 1408 4-aminophenylS(O)₂NH 2-aminophenylethyl 1409 4-aminophenylS(O)₂NH 2-methylsulfonylamino- phenylethyl 1410 4-aminophenylS(O)₂NH 2-trifluoromethylsulfonyl- amino-phenylethyl 1411 4-aminophenylS(O)₂NH 2-hydroxymethylene- phenylethyl 1412 4-aminophenylS(O)₂NH 2-aminomethylene- phenylethyl 1413 4-aminophenylS(O)₂NH 2-tetrazolephenylethyl 1414 4-aminophenylS(O)₂NH 2-tert-butylamino- sulfonylphenylethyl 1415 4-aminophenylS(O)₂NH 2-aminosulfonyl-phenylethyl 1416 4-aminophenylS(O)₂NH 2-methoxyphenylethyl 1417 4-aminophenylS(O)₂NH 3-aminophenylethyl 1418 4-aminophenylS(O)₂NH 3-methylsulfonylamino- phenylethyl 1419 4-aminophenylS(O)₂NH 3-trifluoromethylsulfonyl- amino-phenylethyl 1420 4-aminophenylS(O)₂NH 3-hydroxymethylene- phenylethyl 1421 4-aminophenylS(O)₂NH 3-aminomethylene- phenylethyl 1422 4-aminophenylS(O)₂NH 3-tetrazolephenylethyl 1423 4-aminophenylS(O)₂NH 3-tert-butylamino- sulfonylphenylethyl 1424 4-aminophenylS(O)₂NH 3-aminosulfonyl-phenylethyl 1425 4-aminophenylS(O)₂NH 3-methoxyphenylethyl 1426 NH(CO)NMe₂ H 1427 NH(CO)NMe₂ methyl 1428 NH(CO)NMe₂ ethyl 1429 NH(CO)NMe₂ n-propyl 1430 NH(CO)NMe₂ n-butyl 1431 NH(CO)NMe₂ n-pentyl 1432 NH(CO)NMe₂ n-hexanyl 1433 NH(CO)NMe₂ n-heptanyl 1434 NH(CO)NMe₂ isopropyl 1435 NH(CO)NMe₂ tert-butyl 1436 NH(CO)NMe₂ cyclopropyl 1437 NH(CO)NMe₂ cyclobutanyl 1438 NH(CO)NMe₂ cyclpentanyl 1439 NH(CO)NMe₂ cyclohexanyl 1440 NH(CO)NMe₂ cycloheptanyl 1441 NH(CO)NMe₂ phenyl 1442 NH(CO)NMe₂ phenylmethyl 1443 NH(CO)NMe₂ 3-hydroxyphenyl 1444 NH(CO)NMe₂ 3-hydroxy-4-methoxyphenyl 1445 NH(CO)NMe₂ 3-fluorophenyl 1446 NH(CO)NMe₂ 3-chlorophenyl 1447 NH(CO)NMe₂ 3-nitrophenyl 1448 NH(CO)NMe₂ 3-aminophenyl 1449 NH(CO)NMe₂ 3-methylsulfonamidephenyl 1450 NH(CO)NMe₂ 3-trifluoro- methylsulfonamidephenyl 1451 NH(CO)NMe₂ 3-Ac—NHphenyl 1452 NH(CO)NMe₂ 3-Boc—NHphenyl 1453 NH(CO)NMe₂ 3-Cbz—NHphenyl 1454 NH(CO)NMe₂ 3-aminomethylenephenyl 1455 NH(CO)NMe₂ 3-aminoethylenephenyl 1456 NH(CO)NMe₂ 3-cyanophenyl 1457 NH(CO)NMe₂ 3-cyanomethylphenyl 1458 NH(CO)NMe₂ 3-hydroxymethylenephenyl 1459 NH(CO)NMe₂ 3-carboxylphenyl 1460 NH(CO)NMe₂ 3-mercaptophenyl 1461 NH(CO)NMe₂ 3-methoxyphenyl 1462 NH(CO)NMe₂ 3,4-methylenedioxophenyl 1463 NH(CO)NMe₂ 3-tetrazolephenyl 1464 NH(CO)NMe₂ 3-aminosulfonylphenyl 1465 NH(CO)NMe₂ 3-methylamino- sulfonylphenyl 1466 NH(CO)NMe₂ 3-ethylamino-sulfonylphenyl 1467 NH(CO)NMe₂ 3-tert-butylamino- sulfonylphenyl 1468 NH(CO)NMe₂ 3-methylsulfonylphenyl 1469 NH(CO)NMe₂ 4-methoxyphenyl 1470 NH(CO)NMe₂ 4-phenylphenyl 1471 NH(CO)NMe₂ 4-(2-hydroxy- methylenephenyl)-phenyl 1472 NH(CO)NMe₂ 4-(2-tert-butylamino- sufonylphenyl)-phenyl 1473 NH(CO)NMe₂ 4-(2-methylamino- sufonylphenyl)-phenyl 1474 NH(CO)NMe₂ 4-(2-ethylamino- sufonylphenyl)-phenyl 1475 NH(CO)NMe₂ 4-(2-aminosufonyl-phenyl)- phenyl 1476 NH(CO)NMe₂ 4-(2-chlorophenyl)-phenyl 1477 NH(CO)NMe₂ 4-(2-fluorophenyl)-phenyl 1478 NH(CO)NMe₂ 4-(2,4-dichlorophenyl)-phenyl 1479 NH(CO)NMe₂ 4-(2,6-dichlorophenyl)-phenyl 1480 NH(CO)NMe₂ 4-(3,5-dichlorophenyl)-phenyl 1481 NH(CO)NMe₂ 4-(2,3-dichlorophenyl)-phenyl 1482 NH(CO)NMe₂ 4-(2-methylphenyl)-phenyl 1483 NH(CO)NMe₂ 4-(2-tetrazole-phenyl)-phenyl 1484 NH(CO)NMe₂ 4-(2-methoxy-phenyl)-phenyl 1485 NH(CO)NMe₂ 4-(2-tmethyl-phenyl)-phenyl 1486 NH(CO)NMe₂ 4-(2-formyl-phenyl)-phenyl 1487 NH(CO)NMe₂ 4-(2-amino-phenyl)-phenyl 1488 NH(CO)NMe₂ 4-(2-methylamino-phenyl)- phenyl 1489 NH(CO)NMe₂ 4-(2-ethylamino-phenyl)- phenyl 1490 NH(CO)NMe₂ 4-(2-propylamino-phenyl)- phenyl 1491 NH(CO)NMe₂ 4-(2-methylsulfonylamino- phenyl)-phenyl 1492 NH(CO)NMe₂ 4-(2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1493 NH(CO)NMe₂ 4-(3-methylphenyl)-phenyl 1494 NH(CO)NMe₂ 4-(3-isopropylphenyl)-phenyl 1495 NH(CO)NMe₂ 4-(3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1496 NH(CO)NMe₂ 4-(3-methylsulfonylamino- phenyl)-phenyl 1497 NH(CO)NMe₂ 4-(3-amino-phenyl)-phenyl 1498 NH(CO)NMe₂ 4-(3-nitro-phenyl)-phenyl 1499 NH(CO)NMe₂ 2-pyridyl 1500 NH(CO)NMe₂ 3-pyridyl 1501 NH(CO)NMe₂ 4-pyridyl 1502 NH(CO)NMe₂ 3-amino-4-pyridyl 1503 NH(CO)NMe₂ 3-hydroxy-4-pyridyl 1504 NH(CO)NMe₂ 3-imidazole 1505 NH(CO)NMe₂ 2-nitro-3-imidazole 1506 NH(CO)NMe₂ 5-thiazole 1507 NH(CO)NMe₂ 5-oxazole 1508 NH(CO)NMe₂ 4-pyazole 1509 NH(CO)NMe₂ phenylethyl 1510 NH(CO)NMe₂ 2-aminophenylethyl 1511 NH(CO)NMe₂ 2-methylsulfonylamino- phenylethyl 1512 NH(CO)NMe₂ 2-trifluoromethylsulfonyl- amino-phenylethyl 1513 NH(CO)NMe₂ 2-hydroxymethylene- phenylethyl 1514 NH(CO)NMe₂ 2-aminomethylene- phenylethyl 1515 NH(CO)NMe₂ 2-tetrazolephenylethyl 1516 NH(CO)NMe₂ 2-tert-butylamino- sulfonylphenylethyl 1517 NH(CO)NMe₂ 2-aminosulfonyl-phenylethyl 1518 NH(CO)NMe₂ 2-methoxyphenylethyl 1519 NH(CO)NMe₂ 3-aminophenylethyl 1520 NH(CO)NMe₂ 3-methylsulfonylamino- phenylethyl 1521 NH(CO)NMe₂ 3-trifluoromethylsulfonyl- amino-phenylethyl 1522 NH(CO)NMe₂ 3-hydroxymethylene- phenylethyl 1523 NH(CO)NMe₂ 3-aminomethylene- phenylethyl 1524 NH(CO)NMe₂ 3-tetrazolephenylethyl 1525 NH(CO)NMe₂ 3-tert-butylamino- sulfonylphenylethyl 1526 NH(CO)NMe₂ 3-aminosulfonyl-phenylethyl 1527 NH(CO)NMe₂ 3-methoxyphenylethyl 1528 NH(CO)N(CH₂CH₂)₂O H 1529 NH(CO)N(CH₂CH₂)₂O methyl 1530 NH(CO)N(CH₂CH₂)₂O ethyl 1531 NH(CO)N(CH₂CH₂)₂O n-propyl 1532 NH(CO)N(CH₂CH₂)₂O n-butyl 1533 NH(CO)N(CH₂CH₂)₂O n-pentyl 1534 NH(CO)N(CH₂CH₂)₂O n-hexanyl 1535 NH(CO)N(CH₂CH₂)₂O n-heptanyl 1536 NH(CO)N(CH₂CH₂)₂O isopropyl 1537 NH(CO)N(CH₂CH₂)₂O tert-butyl 1538 NH(CO)N(CH₂CH₂)₂O cyclopropyl 1539 NH(CO)N(CH₂CH₂)₂O cyclobutanyl 1540 NH(CO)N(CH₂CH₂)₂O cyclpentanyl 1541 NH(CO)N(CH₂CH₂)₂O cyclohexanyl 1542 NH(CO)N(CH₂CH₂)₂O cycloheptanyl 1543 NH(CO)N(CH₂CH₂)₂O phenyl 1544 NH(CO)N(CH₂CH₂)₂O phenylmethyl 1545 NH(CO)N(CH₂CH₂)₂O 3-hydroxyphenyl 1546 NH(CO)N(CH₂CH₂)₂O 3-hydroxy-4-methoxyphenyl 1547 NH(CO)N(CH₂CH₂)₂O 3-fluorophenyl 1548 NH(CO)N(CH₂CH₂)₂O 3-chlorophenyl 1549 NH(CO)N(CH₂CH₂)₂O 3-nitrophenyl 1550 NH(CO)N(CH₂CH₂)₂O 3-aminophenyl 1551 NH(CO)N(CH₂CH₂)₂O 3-methyl-sulfonamidephenyl 1552 NH(CO)N(CH₂CH₂)₂O 3-trifluoro- methylsulfonamidephenyl 1553 NH(CO)N(CH₂CH₂)₂O 3-Ac—NHphenyl 1554 NH(CO)N(CH₂CH₂)₂O 3-Boc—NHphenyl 1555 NH(CO)N(CH₂CH₂)₂O 3-Cbz—NHphenyl 1556 NH(CO)N(CH₂CH₂)₂O 3-aminomethylenephenyl 1557 NH(CO)N(CH₂CH₂)₂O 3-aminoethylenephenyl 1558 NH(CO)N(CH₂CH₂)₂O 3-cyanophenyl 1559 NH(CO)N(CH₂CH₂)₂O 3-cyanomethylphenyl 1560 NH(CO)N(CH₂CH₂)₂O 3-hydroxymethylenephenyl 1561 NH(CO)N(CH₂CH₂)₂O 3-carboxylphenyl 1562 NH(CO)N(CH₂CH₂)₂O 3-mercaptophenyl 1563 NH(CO)N(CH₂CH₂)₂O 3-methoxyphenyl 1564 NH(CO)N(CH₂CH₂)₂O 3,4-methylenedioxophenyl 1565 NH(CO)N(CH₂CH₂)₂O 3-tetrazolephenyl 1566 NH(CO)N(CH₂CH₂)₂O 3-aminosulfonylphenyl 1567 NH(CO)N(CH₂CH₂)₂O 3-methylamino- sulfonylphenyl 1568 NH(CO)N(CH₂CH₂)₂O 3-ethylamino-sulfonylphenyl 1569 NH(CO)N(CH₂CH₂)₂O 3-tert-butylamino- sulfonylphenyl 1570 NH(CO)N(CH₂CH₂)₂O 3-methylsulfonylphenyl 1571 NH(CO)N(CH₂CH₂)₂O 4-methoxyphenyl 1572 NH(CO)N(CH₂CH₂)₂O 4-phenylphenyl 1573 NH(CO)N(CH₂CH₂)₂O 4-(2-hydroxy- methylenephenyl)-phenyl 1574 NH(CO)N(CH₂CH₂)₂O 4-(2-tert-butylamino- sufonylphenyl)-phenyl 1575 NH(CO)N(CH₂CH₂)₂O 4-(2-methylamino- sufonylphenyl)-phenyl 1576 NH(CO)N(CH₂CH₂)₂O 4-(2-ethylamino- sufonylphenyl)-phenyl 1577 NH(CO)N(CH₂CH₂)₂O 4-(2-aminosufonyl-phenyl)- phenyl 1578 NH(CO)N(CH₂CH₂)₂O 4-(2-chlorophenyl)-phenyl 1579 NH(CO)N(CH₂CH₂)₂O 4-(2-fluorophenyl)-phenyl 1580 NH(CO)N(CH₂CH₂)₂O 4-(2,4-dichlorophenyl)-phenyl 1581 NH(CO)N(CH₂CH₂)₂O 4-(2,6-dichlorophenyl)-phenyl 1582 NH(CO)N(CH₂CH₂)₂O 4-(3,5-dichlorophenyl)-phenyl 1583 NH(CO)N(CH₂CH₂)₂O 4-(2,3-dichlorophenyl)-phenyl 1584 NH(CO)N(CH₂CH₂)₂O 4-(2-methylphenyl)-phenyl 1585 NH(CO)N(CH₂CH₂)₂O 4-(2-tetrazole-phenyl)-phenyl 1586 NH(CO)N(CH₂CH₂)₂O 4-(2-methoxy-phenyl)-phenyl 1587 NH(CO)N(CH₂CH₂)₂O 4-(2-tmethyl-phenyl)-phenyl 1588 NH(CO)N(CH₂CH₂)₂O 4-(2-formyl-phenyl)-phenyl 1589 NH(CO)N(CH₂CH₂)₂O 4-(2-amino-phenyl)-phenyl 1590 NH(CO)N(CH₂CH₂)₂O 4-(2-methylamino-phenyl)- phenyl 1591 NH(CO)N(CH₂CH₂)₂O 4-(2-ethylamino-phenyl)- phenyl 1592 NH(CO)N(CH₂CH₂)₂O 4-(2-propylamino-phenyl)- phenyl 1593 NH(CO)N(CH₂CH₂)₂O 4-(2-methylsulfonylamino- phenyl)-phenyl 1594 NH(CO)N(CH₂CH₂)₂O 4-(2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1595 NH(CO)N(CH₂CH₂)₂O 4-(3-methylphenyl)-phenyl 1596 NH(CO)N(CH₂CH₂)₂O 4-(3-isopropylphenyl)-phenyl 1597 NH(CO)N(CH₂CH₂)₂O 4-(3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1598 NH(CO)N(CH₂CH₂)₂O 4-(3-methylsulfonylamino- phenyl)-phenyl 1599 NH(CO)N(CH₂CH₂)₂O 4-(3-amino-phenyl)-phenyl 1600 NH(CO)N(CH₂CH₂)₂O 4-(3-nitro-phenyl)-phenyl 1601 NH(CO)N(CH₂CH₂)₂O 2-pyridyl 1602 NH(CO)N(CH₂CH₂)₂O 3-pyridyl 1603 NH(CO)N(CH₂CH₂)₂O 4-pyridyl 1604 NH(CO)N(CH₂CH₂)₂O 3-amino-4-pyridyl 1605 NH(CO)N(CH₂CH₂)₂O 3-hydroxy-4-pyridyl 1606 NH(CO)N(CH₂CH₂)₂O 3-imidazole 1607 NH(CO)N(CH₂CH₂)₂O 2-nitro-3-imidazole 1608 NH(CO)N(CH₂CH₂)₂O 5-thiazole 1609 NH(CO)N(CH₂CH₂)₂O 5-oxazole 1610 NH(CO)N(CH₂CH₂)₂O 4-pyazole 1611 NH(CO)N(CH₂CH₂)₂O phenylethyl 1612 NH(CO)N(CH₂CH₂)₂O 2-aminophenylethyl 1613 NH(CO)N(CH₂CH₂)₂O 2-methylsulfonylamino- phenylethyl 1614 NH(CO)N(CH₂CH₂)₂O 2-trifluoromethylsulfonyl- amino-phenylethyl 1615 NH(CO)N(CH₂CH₂)₂O 2-hydroxymethylene- phenylethyl 1616 NH(CO)N(CH₂CH₂)₂O 2-aminomethylene- phenylethyl 1617 NH(CO)N(CH₂CH₂)₂O 2-tetrazolephenylethyl 1618 NH(CO)N(CH₂CH₂)₂O 2-tert-butylamino- sulfonylphenylethyl 1619 NH(CO)N(CH₂CH₂)₂O 2-aminosulfonyl-phenylethyl 1620 NH(CO)N(CH₂CH₂)₂O 2-methoxyphenylethyl 1621 NH(CO)N(CH₂CH₂)₂O 3-aminophenylethyl 1622 NH(CO)N(CH₂CH₂)₂O 3-methylsulfonylamino- phenylethyl 1623 NH(CO)N(CH₂CH₂)₂O 3-trifluoromethylsulfonyl- amino-phenylethyl 1624 NH(CO)N(CH₂CH₂)₂O 3-hydroxymethylene- phenylethyl 1625 NH(CO)N(CH₂CH₂)₂O 3-aminomethylene- phenylethyl 1626 NH(CO)N(CH₂CH₂)₂O 3-tetrazolephenylethyl 1627 NH(CO)N(CH₂CH₂)₂O 3-tert-butylamino- sulfonylphenylethyl 1628 NH(CO)N(CH₂CH₂)₂O 3-aminosulfonyl-phenylethyl 1629 NH(CO)N(CH₂CH₂)₂O 3-methoxyphenylethyl 1630 tert-BuCONH H 1631 tert-BuCONH methyl 1632 tert-BuCONH ethyl 1633 tert-BuCONH n-propyl 1634 tert-BuCONH n-butyl 1635 tert-BuCONH n-pentyl 1636 tert-BuCONH n-hexanyl 1637 tert-BuCONH n-heptanyl 1638 tert-BuCONH isopropyl 1639 tert-BuCONH tert-butyl 1640 tert-BuCONH cyclopropyl 1641 tert-BuCONH cyclobutanyl 1642 tert-BuCONH cyclpentanyl 1643 tert-BuCONH cyclohexanyl 1644 tert-BuCONH cycloheptanyl 1645 tert-BuCONH phenyl 1646 tert-BuCONH phenylmethyl 1647 tert-BuCONH 3-hydroxyphenyl 1648 tert-BuCONH 3-hydroxy-4-methoxyphenyl 1649 tert-BuCONH 3-fluorophenyl 1650 tert-BuCONH 3-chlorophenyl 1651 tert-BuCONH 3-nitrophenyl 1652 tert-BuCONH 3-aminophenyl 1653 tert-BuCONH 3-methyl-sulfonamidephenyl 1654 tert-BuCONH 3-trifluoro- methylsulfonamidephenyl 1655 tert-BuCONH 3-Ac—NHphenyl 1656 tert-BuCONH 3-Boc—NHphenyl 1657 tert-BuCONH 3-Cbz—NHphenyl 1658 tert-BuCONH 3-aminomethylenephenyl 1659 tert-BuCONH 3-aminoethylenephenyl 1660 tert-BuCONH 3-cyanophenyl 1661 tert-BuCONH 3-cyanomethylphenyl 1662 tert-BuCONH 3-hydroxymethylenephenyl 1663 tert-BuCONH 3-carboxylphenyl 1664 tert-BuCONH 3-mercaptophenyl 1665 tert-BuCONH 3-methoxyphenyl 1666 tert-BuCONH 3,4-methylenedioxophenyl 1667 tert-BuCONH 3-tetrazolephenyl 1668 tert-BuCONH 3-aminosulfonylphenyl 1669 tert-BuCONH 3-methylamino- sulfonylphenyl 1670 tert-BuCONH 3-ethylamino-sulfonylphenyl 1671 tert-BuCONH 3-tert-butylamino- sulfonylphenyl 1672 tert-BuCONH 3-methylsulfonylphenyl 1673 tert-BuCONH 4-methoxyphenyl 1674 tert-BuCONH 4-phenylphenyl 1675 tert-BuCONH 4-(2-hydroxy- methylenephenyl)-phenyl 1676 tert-BuCONH 4-(2-tert-butylamino- sufonylphenyl)-phenyl 1677 tert-BuCONH 4-(2-methylamino- sufonylphenyl)-phenyl 1678 tert-BuCONH 4-(2-ethylamino- sufonylphenyl)-phenyl 1679 tert-BuCONH 4-(2-aminosufonyl-phenyl)- phenyl 1680 tert-BuCONH 4-(2-chlorophenyl)-phenyl 1681 tert-BuCONH 4-(2-fluorophenyl)-phenyl 1682 tert-BuCONH 4-(2,4-dichlorophenyl)-phenyl 1683 tert-BuCONH 4-(2,6-dichlorophenyl)-phenyl 1684 tert-BuCONH 4-(3,5-dichlorophenyl)-phenyl 1685 tert-BuCONH 4-(2,3-dichlorophenyl)-phenyl 1686 tert-BuCONH 4-(2-methylphenyl)-phenyl 1687 tert-BuCONH 4-(2-tetrazole-phenyl)-phenyl 1688 tert-BuCONH 4-(2-methoxy-phenyl)-phenyl 1689 tert-BuCONH 4-(2-tmethyl-phenyl)-phenyl 1690 tert-BuCONH 4-(2-formyl-phenyl)-phenyl 1691 tert-BuCONH 4-(2-amino-phenyl)-phenyl 1692 tert-BuCONH 4-(2-methylamino-phenyl)- phenyl 1693 tert-BuCONH 4-(2-ethylamino-phenyl)- phenyl 1694 tert-BuCONH 4-(2-propylamino-phenyl)- phenyl 1695 tert-BuCONH 4-(2-methylsulfonylamino- phenyl)-phenyl 1696 tert-BuCONH 4-(2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1697 tert-BuCONH 4-(3-methylphenyl)-phenyl 1698 tert-BuCONH 4-(3-isopropylphenyl)-phenyl 1699 tert-BuCONH 4-(3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1700 tert-BuCONH 4-(3-methylsulfonylamino- phenyl)-phenyl 1701 tert-BuCONH 4-(3-amino-phenyl)-phenyl 1702 tert-BuCONH 4-(3-nitro-phenyl)-phenyl 1703 tert-BuCONH 2-pyridyl 1704 tert-BuCONH 3-pyridyl 1705 tert-BuCONH 4-pyridyl 1706 tert-BuCONH 3-amino-4-pyridyl 1707 tert-BuCONH 3-hydroxy-4-pyridyl 1708 tert-BuCONH 3-imidazole 1709 tert-BuCONH 2-nitro-3-imidazole 1710 tert-BuCONH 5-thiazole 1711 tert-BuCONH 5-oxazole 1712 tert-BuCONH 4-pyazole 1713 tert-BuCONH phenylethyl 1714 tert-BuCONH 2-aminophenylethyl 1715 tert-BuCONH 2-methylsulfonylamino- phenylethyl 1716 tert-BuCONH 2-trifluoromethylsulfonyl- amino-phenylethyl 1717 tert-BuCONH 2-hydroxymethylene- phenylethyl 1718 tert-BuCONH 2-aminomethylene- phenylethyl 1719 tert-BuCONH 2-tetrazolephenylethyl 1720 tert-BuCONH 2-tert-butylamino- sulfonylphenylethyl 1721 tert-BuCONH 2-aminosulfonyl-phenylethyl 1722 tert-BuCONH 2-methoxyphenylethyl 1723 tert-BuCONH 3-aminophenylethyl 1724 tert-BuCONH 3-methylsulfonylamino- phenylethyl 1725 tert-BuCONH 3-trifluoromethylsulfonyl- amino-phenylethyl 1726 tert-BuCONH 3-hydroxymethylene- phenylethyl 1727 tert-BuCONH 3-aminomethylene- phenylethyl 1728 tert-BuCONH 3-tetrazolephenylethyl 1729 tert-BuCONH 3-tert-butylamino- sulfonylphenylethyl 1730 tert-BuCONH 3-aminosulfonyl-phenylethyl 1731 tert-BuCONH 3-methoxyphenylethyl 1732 c-C₃H₅CONH H 1733 c-C₃H₅CONH methyl 1734 c-C₃H₅CONH ethyl 1735 c-C₃H₅CONH n-propyl 1736 c-C₃H₅CONH n-butyl 1737 c-C₃H₅CONH n-pentyl 1738 c-C₃H₅CONH n-hexanyl 1739 c-C₃H₅CONH n-heptanyl 1740 c-C₃H₅CONH isopropyl 1741 c-C₃H₅CONH tert-butyl 1742 c-C₃H₅CONH cyclopropyl 1743 c-C₃H₅CONH cyclobutanyl 1744 c-C₃H₅CONH cyclpentanyl 1745 c-C₃H₅CONH cyclohexanyl 1746 c-C₃H₅CONH cycloheptanyl 1747 c-C₃H₅CONH phenyl 1748 c-C₃H₅CONH phenylmethyl 1749 c-C₃H₅CONH 3-hydroxyphenyl 1750 c-C₃H₅CONH 3-hydroxy-4-methoxyphenyl 1751 c-C₃H₅CONH 3-fluorophenyl 1752 c-C₃H₅CONH 3-chlorophenyl 1753 c-C₃H₅CONH 3-nitrophenyl 1754 c-C₃H₅CONH 3-aminophenyl 1755 c-C₃H₅CONH 3-methyl-sulfonamidephenyl 1756 c-C₃H₅CONH 3-trifluoro- methylsulfonamidephenyl 1757 c-C₃H₅CONH 3-Ac—NHphenyl 1758 c-C₃H₅CONH 3-Boc—NHphenyl 1759 c-C₃H₅CONH 3-Cbz—NHphenyl 1760 c-C₃H₅CONH 3-aminomethylenephenyl 1761 c-C₃H₅CONH 3-aminoethylenephenyl 1762 c-C₃H₅CONH 3-cyanophenyl 1763 c-C₃H₅CONH 3-cyanomethylphenyl 1764 c-C₃H₅CONH 3-hydroxymethylenephenyl 1765 c-C₃H₅CONH 3-carboxylphenyl 1766 c-C₃H₅CONH 3-mercaptophenyl 1767 c-C₃H₅CONH 3-methoxyphenyl 1768 c-C₃H₅CONH 3,4-methylenedioxophenyl 1769 c-C₃H₅CONH 3-tetrazolephenyl 1770 c-C₃H₅CONH 3-aminosulfonylphenyl 1771 c-C₃H₅CONH 3-methylamino- sulfonylphenyl 1772 c-C₃H₅CONH 3-ethylamino-sulfonylphenyl 1773 c-C₃H₅CONH 3-tert-butylamino- sulfonylphenyl 1774 c-C₃H₅CONH 3-methylsulfonylphenyl 1775 c-C₃H₅CONH 4-methoxyphenyl 1776 c-C₃H₅CONH 4-phenylphenyl 1777 c-C₃H₅CONH 4-(2-hydroxy- methylenephenyl)-phenyl 1778 c-C₃H₅CONH 4-(2-tert-butylamino- sufonylphenyl)-phenyl 1779 c-C₃H₅CONH 4-(2-methylamino- sufonylphenyl)-phenyl 1780 c-C₃H₅CONH 4-(2-ethylamino- sufonylphenyl)-phenyl 1781 c-C₃H₅CONH 4-(2-aminosufonyl-phenyl)- phenyl 1782 c-C₃H₅CONH 4-(2-chlorophenyl)-phenyl 1783 c-C₃H₅CONH 4-(2-fluorophenyl)-phenyl 1784 c-C₃H₅CONH 4-(2,4-dichlorophenyl)-phenyl 1785 c-C₃H₅CONH 4-(2,6-dichlorophenyl)-phenyl 1786 c-C₃H₅CONH 4-(3,5-dichlorophenyl)-phenyl 1787 c-C₃H₅CONH 4-(2,3-dichlorophenyl)-phenyl 1788 c-C₃H₅CONH 4-(2-methylphenyl)-phenyl 1789 c-C₃H₅CONH 4-(2-tetrazole-phenyl)-phenyl 1790 c-C₃H₅CONH 4-(2-methoxy-phenyl)-phenyl 1791 c-C₃H₅CONH 4-(2-tmethyl-phenyl)-phenyl 1792 c-C₃H₅CONH 4-(2-formyl-phenyl)-phenyl 1793 c-C₃H₅CONH 4-(2-amino-phenyl)-phenyl 1794 c-C₃H₅CONH 4-(2-methylamino-phenyl)- phenyl 1795 c-C₃H₅CONH 4-(2-ethylamino-phenyl)- phenyl 1796 c-C₃H₅CONH 4-(2-propylamino-phenyl)- phenyl 1797 c-C₃H₅CONH 4-(2-methylsulfonylamino- phenyl)-phenyl 1798 c-C₃H₅CONH 4-(2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1799 c-C₃H₅CONH 4-(3-methylphenyl)-phenyl 1800 c-C₃H₅CONH 4-(3-isopropylphenyl)-phenyl 1801 c-C₃H₅CONH 4-(3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1802 c-C₃H₅CONH 4-(3-methylsulfonylamino- phenyl)-phenyl 1803 c-C₃H₅CONH 4-(3-amino-phenyl)-phenyl 1804 c-C₃H₅CONH 4-(3-nitro-phenyl)-phenyl 1805 c-C₃H₅CONH 2-pyridyl 1806 c-C₃H₅CONH 3-pyridyl 1807 c-C₃H₅CONH 4-pyridyl 1808 c-C₃H₅CONH 3-amino-4-pyridyl 1809 c-C₃H₅CONH 3-hydroxy-4-pyridyl 1810 c-C₃H₅CONH 3-imidazole 1811 c-C₃H₅CONH 2-nitro-3-imidazole 1812 c-C₃H₅CONH 5-thiazole 1813 c-C₃H₅CONH 5-oxazole 1814 c-C₃H₅CONH 4-pyazole 1815 c-C₃H₅CONH phenylethyl 1816 c-C₃H₅CONH 2-aminophenylethyl 1817 c-C₃H₅CONH 2-methylsulfonylamino- phenylethyl 1818 c-C₃H₅CONH 2-trifluoromethylsulfonyl- amino-phenylethyl 1819 c-C₃H₅CONH 2-hydroxymethylene- phenylethyl 1820 c-C₃H₅CONH 2-aminomethylene- phenylethyl 1821 c-C₃H₅CONH 2-tetrazolephenylethyl 1822 c-C₃H₅CONH 2-tert-butylamino- sulfonylphenylethyl 1823 c-C₃H₅CONH 2-aminosulfonyl-phenylethyl 1824 c-C₃H₅CONH 2-methoxyphenylethyl 1825 c-C₃H₅CONH 3-aminophenylethyl 1826 c-C₃H₅CONH 3-methylsulfonylamino- phenylethyl 1827 c-C₃H₅CONH 3-trifluoromethylsulfonyl- amino-phenylethyl 1828 c-C₃H₅CONH 3-hydroxymethylene- phenylethyl 1829 c-C₃H₅CONH 3-aminomethylene- phenylethyl 1830 c-C₃H₅CONH 3-tetrazolephenylethyl 1831 c-C₃H₅CONH 3-tert-butylamino- sulfonylphenylethyl 1832 c-C₃H₅CONH 3-aminosulfonyl-phenylethyl 1833 c-C₃H₅CONH 3-methoxyphenylethyl 1834 1835 H 1836 ″ methyl 1837 ″ ethyl 1838 ″ n-propyl 1839 ″ n-butyl 1840 ″ n-pentyl 1841 ″ n-hexanyl 1842 ″ n-heptanyl 1843 ″ isopropyl 1844 ″ tert-butyl 1845 ″ cyclopropyl 1846 ″ cyclobutanyl 1847 ″ cyclpentanyl 1848 ″ cyclohexanyl 1849 ″ cycloheptanyl 1850 ″ phenyl 1851 ″ phenylmethyl 1852 ″ 3-hydroxyphenyl 1853 ″ 3-hydroxy-4-methoxyphenyl 1854 ″ 3-fluorophenyl 1855 ″ 3-chlorophenyl 1856 ″ 3-nitrophenyl 1857 ″ 3-aminophenyl 1858 ″ 3-methyl-sulfonamidephenyl 1859 ″ 3-trifluoro- methylsulfonamidephenyl 1860 ″ 3-Ac—NHphenyl 1861 ″ 3-Boc—NHphenyl 1862 ″ 3-Cbz—NHphenyl 1863 ″ 3-aminomethylenephenyl 1864 ″ 3-aminoethylenephenyl 1865 ″ 3-cyanophenyl 1866 ″ 3-cyanomethylphenyl 1867 ″ 3-hydroxymethylenephenyl 1868 ″ 3-carboxylphenyl 1869 ″ 3-mercaptophenyl 1870 ″ 3-methoxyphenyl 1871 ″ 3,4-methylenedioxophenyl 1872 ″ 3-tetrazolephenyl 1873 ″ 3-aminosulfonylphenyl 1874 ″ 3-methylamino- sulfonylphenyl 1875 ″ 3-ethylamino-sulfonylphenyl 1876 ″ 3-tert-butylamino- sulfonylphenyl 1877 ″ 3-methylsulfonylphenyl 1878 ″ 4-methoxyphenyl 1879 ″ 4-phenylphenyl 1880 ″ 4-(2-hydroxy- methylenephenyl)-phenyl 1881 ″ 4-(2-tert-butylamino- sufonylphenyl)-phenyl 1882 ″ 4-(2-methylamino- sufonylphenyl)-phenyl 1883 ″ 4-(2-ethylamino- sufonylphenyl)-phenyl 1884 ″ 4-(2-aminosufonyl-phenyl)- phenyl 1885 ″ 4-(2-chlorophenyl)-phenyl 1886 ″ 4-(2-fluorophenyl)-phenyl 1887 ″ 4-(2,4-dichlorophenyl)-phenyl 1888 ″ 4-(2,6-dichlorophenyl)-phenyl 1889 ″ 4-(3,5-dichlorophenyl)-phenyl 1890 ″ 4-(2,3-dichlorophenyl)-phenyl 1891 ″ 4-(2-methylphenyl)-phenyl 1892 ″ 4-(2-tetrazole-phenyl)-phenyl 1893 ″ 4-(2-methoxy-phenyl)-phenyl 1894 ″ 4-(2-tmethyl-phenyl)-phenyl 1895 ″ 4-(2-formyl-phenyl)-phenyl 1896 ″ 4-(2-amino-phenyl)-phenyl 1897 ″ 4-(2-methylamino-phenyl)- phenyl 1898 ″ 4-(2-ethylamino-phenyl)- phenyl 1899 ″ 4-(2-propylamino-phenyl)- phenyl 1900 ″ 4-(2-methylsulfonylamino- phenyl)-phenyl 1901 ″ 4-(2-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1902 ″ 4-(3-methylphenyl)-phenyl 1903 ″ 4-(3-isopropylphenyl)-phenyl 1904 ″ 4-(3-trifluoromethyl- sulfonyl-amino-phenyl)- phenyl 1905 ″ 4-(3-methylsulfonylamino- phenyl)-phenyl 1906 ″ 4-(3-amino-phenyl)-phenyl 1907 ″ 4-(3-nitro-phenyl)-phenyl 1908 ″ 2-pyridyl 1909 ″ 3-pyridyl 1910 ″ 4-pyridyl 1911 ″ 3-amino-4-pyridyl 1912 ″ 3-hydroxy-4-pyridyl 1913 ″ 3-imidazole 1914 ″ 2-nitro-3-imidazole 1915 ″ 5-thiazole 1916 ″ 5-oxazole 1917 ″ 4-pyazole 1918 ″ phenylethyl 1919 ″ 2-aminophenylethyl 1920 ″ 2-methylsulfonylamino- phenylethyl 1921 ″ 2-trifluoromethylsulfonyl- amino-phenylethyl 1922 ″ 2-hydroxymethylene- phenylethyl 1923 ″ 2-aminomethylene- phenylethyl 1924 ″ 2-tetrazolephenylethyl 1925 ″ 2-tert-butylamino- sulfonylphenylethyl 1926 ″ 2-aminosulfonyl-phenylethyl 1927 ″ 2-methoxyphenylethyl 1928 ″ 3-aminophenylethyl 1929 ″ 3-methylsulfonylamino- phenylethyl 1930 ″ 3-trifluoromethylsulfonyl- amino-phenylethyl 1931 ″ 3-hydroxymethylene- phenylethyl 1932 ″ 3-aminomethylene- phenylethyl 1933 ″ 3-tetrazolephenylethyl 1934 ″ 3-tert-butylamino- sulfonylphenylethyl 1935 ″ 3-aminosulfonyl-phenylethyl 1936 ″ 3-methoxyphenylethyl

TABLE 3

I

II

III

IV

V

VI

VII

VIII

IX

X

XI

XII

XIII

XIV

XV

XVI

XVII

XVIII

XIX

XX

XXI

XXII

XXIII

XXIV

XXV

XXVI

XXVII Ex # R3 Ms Ex # R3 Ms 2000 H 2001 4-(2- aminosufonylphenyl)- phenyl 2002 methyl 2003 4-(2-chlorophenyl)- phenyl 2004 ethyl 2005 4-(2-fluorophenyl)- phenyl 2006 n-propyl 2007 4-(2,4- dichlorophenyl)-phenyl 2008 n-butyl 2009 4-(2,6- dichlorophenyl)-phenyl 2010 n-pentyl 2011 4-(3,5- dichlorophenyl)-phenyl 2012 n-hexanyl 2013 4-(2,3- dichlorophenyl)-phenyl 2014 n-heptanyl 2015 4-(2-methylphenyl)- phenyl 2016 isopropyl 2017 4-(2-tetrazole- phenyl)-phenyl 2018 tert-butyl 2019 4-(2-methoxy-phenyl)- phenyl 2020 cyclopropyl 2021 4-(2-tmethyl-phenyl)- phenyl 2022 cyclobutanyl 2023 4-(2-formyl-phenyl)- phenyl 2024 cyclpentanyl 2025 4-(2-amino-phenyl)- phenyl 2026 cyclohexanyl 2027 4-(2-methylamino- phenyl)-phenyl 2028 cycloheptanyl 2029 4-(2-ethylamino- phenyl)-phenyl 2030 phenyl 2031 4-(2-propylamino- phenyl)-phenyl 2032 phenylmethyl 2033 4-(2- methylsulfonylamino- phenyl)-phenyl 2034 3-hydroxyphenyl 2035 4-(2- trifluoromethylsulfonyl- amino-phenyl)-phenyl 2036 3-hydroxy-4- 2037 4-(3-methylphenyl)- methoxyphenyl phenyl 2038 3-fluorophenyl 2039 4-(3-isopropylphenyl)- phenyl 2040 3-chlorophenyl 2041 4-(3- trifluoromethylsulfonyl- amino-phenyl)-phenyl 2042 3-nitrophenyl 2043 4-(3- methylsulfonylamino- phenyl)-phenyl 2044 3-aminophenyl 2045 4-(3-amino-phenyl)- phenyl 2046 3-methylsul- 2047 4-(3-nitro-phenyl)- fonamidephenyl phenyl 2048 3-trifluoro-methyl- 2049 2-pyridyl sulfonamidephenyl 2050 3-Ac—NHphenyl 2051 3-pyridyl 2052 3-Boc—NHphenyl 2053 4-pyridyl 2054 3-Cbz—NHphenyl 2055 3-amino-4-pyridyl 2056 3-aminomethylene- 2057 3-hydroxy-4-pyridyl phenyl 2058 3-amino- 2059 3-imidazole ethylenephenyl 2060 3-cyanophenyl 2061 2-nitro-3-imidazole 2062 3-cyanomethylphenyl 2063 5-thiazole 2064 3-hydroxy- 2065 5-oxazole methylenephenyl 2066 3-carboxylphenyl 2067 4-pyazole 2068 3-mercaptophenyl 2069 phenylethyl 2070 3-methoxyphenyl 2071 2-aminophenylethyl 2072 3,4-methylenedioxo- 2073 2-methylsulfonyl- phenyl amino-phenylethyl 2074 3-tetrazolephenyl 2075 2- trifluoromethylsulfonyl- amino-phenylethyl 2076 3-aminosulfonylphenyl 2077 2-hydroxymethylene- phenylethyl 2078 3-methylamino- 2079 2-aminomethylene- sulfonylphenyl phenylethyl 2080 3-ethylamino- 2081 2-tetrazole- sulfonylphenyl phenylethyl 2082 3-tert-butylamino- 2083 2-tertbutylamino- sulfonylphenyl sulfonylphenylethyl 2084 3-methylsulfonyl- 2085 2-aminosulfonyl- phenyl phenylethyl 2086 4-methoxyphenyl 2087 2-methoxy-phenylethyl 2088 4-phenylphenyl 2089 3-aminophenylethyl 2090 4-(2-hydroxymethyl- 2091 3-methylsulfonyl- enephenyl)-phenyl amino-phenylethyl 2092 4-(2-tert-butyl- 2093 3- aminosufonylphenyl)- trifluoromethylsulfonyl- phenyl amino-phenylethyl 2094 4-(2-methylamino- 2095 3-hydroxymethylene- sufonylphenyl)-phenyl phenylethyl 2096 4-(2-ethylamino- 2097 3-aminomethylene- sufonylphenyl)-phenyl phenylethyl 2098 2099 3-tetrazole- phenylethyl 2100 2101 3-tert-butylamino- sulfonylphenylethyl 2102 2103 3-aminosulfonyl- phenylethyl 2104 2105 3-methoxy-phenylethyl

TABLE 4

I

II

III

IV

V

VI Ex # R2 R3 2500 n-Bu H 2501 ″ methyl 2502 ″ ethyl 2503 ″ n-propyl 2504 ″ n-butyl 2505 ″ n-pentyl 2506 ″ n-hexanyl 2507 ″ n-heptanyl 2508 ″ isopropyl 2509 ″ tert-butyl 2510 ″ cyclopropyl 2511 ″ cyclobutanyl 2512 ″ cyclpentanyl 2513 ″ cyclohexanyl 2514 ″ cycloheptanyl 2515 ″ phenyl 2516 ″ phenylmethyl 2517 ″ 3-hydroxyphenyl 2518 ″ 3-hydroxy-4-methoxyphenyl 2519 ″ 3-fluorophenyl 2520 ″ 3-chlorophenyl 2521 ″ 3-nitrophenyl 2522 ″ 3-aminophenyl 2523 ″ 3-methyl-sulfonamidephenyl 2524 ″ 3-trifluoro-methyl- sulfonamidephenyl 2525 ″ 3-Ac—NHphenyl 2526 ″ 3-Boc—NHphenyl 2527 ″ 3-Cbz—NHphenyl 2528 ″ 3-aminomethylenephenyl 2529 ″ 3-aminoethylenephenyl 2530 ″ 3-cyanophenyl 2531 ″ 3-cyanomethylphenyl 2532 ″ 3-hydroxy-methylenephenyl 2533 ″ 3-carboxylphenyl 2534 ″ 3-mercaptophenyl 2535 ″ 3-methoxyphenyl 2536 ″ 3,4-methylene-dioxophenyl 2537 ″ 3-tetrazolephenyl 2538 ″ 3-aminosulfonylphenyl 2539 ″ 3-methylamino- sulfonylphenyl 2540 ″ 3-ethylamino-sulfonylphenyl 2541 ″ 3-tertbutylamino- sulfonylphenyl 2542 ″ 3-methylsulfonylphenyl 2543 ″ 4-methoxyphenyl 2544 ″ 4-phenylphenyl 2545 ″ 4-(2-hydroxymethylene- phenyl)-phenyl 2546 ″ 4-(2-tertbutylamino- sufonylphenyl)-phenyl 2547 ″ 4-(2-methylamino- sufonylphenyl)-phenyl 2548 ″ 4-(2-ethylamino- sufonylphenyl)-phenyl 2549 ″ 4-(2-aminosufonyl-phenyl)- phenyl 2550 ″ 4-(2-chlorophenyl)-phenyl 2551 ″ 4-(2-fluorophenyl)-phenyl 2552 ″ 4-(2,4-dichlorophenyl)- phenyl 2553 ″ 4-(2,6-dichlorophenyl)- phenyl 2554 ″ 4-(3,5-dichlorophenyl)- phenyl 2555 ″ 4-(2,3-dichlorophenyl)- phenyl 2556 ″ 4-(2-methylphenyl)-phenyl 2557 ″ 4-(2-tetrazole-phenyl)- phenyl 2558 ″ 4-(2-methoxy-phenyl)-phenyl 2559 ″ 4-(2-tmethyl-phenyl)-phenyl 2560 ″ 4-(2-formyl-phenyl)-phenyl 2561 ″ 4-(2-amino-phenyl)-phenyl 2562 ″ 4-(2-methylamino-phenyl)- phenyl 2563 ″ 4-(2-ethylamino-phenyl)- phenyl 2564 ″ 4-(2-propylamino-phenyl)- phenyl 2565 ″ 4-(2-methylsulfonylamino- phenyl)-phenyl 2566 ″ 4-(2- trifluoromethylsulfonyl- amino-phenyl)-phenyl 2567 ″ 4-(3-methylphenyl)-phenyl 2568 ″ 4-(3-isopropylphenyl)- phenyl 2569 ″ 4-(3- trifluoromethylsulfonyl- amino-phenyl)-phenyl 2570 ″ 4-(3-methylsulfonylamino- phenyl)-phenyl 2571 ″ 4-(3-amino-phenyl)-phenyl 2572 ″ 4-(3-nitro-phenyl)-phenyl 2573 ″ 2-pyridyl 2574 ″ 3-pyridyl 2575 ″ 4-pyridyl 2576 ″ 3-amino-4-pyridyl 2577 ″ 3-hydroxy-4-pyridyl 2578 ″ 3-imidazole 2579 ″ 2-nitro-3-imidazole 2580 ″ 5-thiazole 2581 ″ 5-oxazole 2582 ″ 4-pyazole 2583 ″ phenylethyl 2584 ″ 2-aminophenylethyl 2585 ″ 2-methylsulfonylamino- phenylethyl 2586 ″ 2-trifluoromethyl- sulfonylamino-phenylethyl 2587 ″ 2-hydroxy- methylenephenylethyl 2588 ″ 2-aminomethylene- phenylethyl 2589 ″ 2-tetrazolephenylethyl 2590 ″ 2-tertbutylamino- sulfonylphenylethyl 2591 ″ 2-aminosulfonyl-phenylethyl 2592 ″ 2-methoxyphenylethyl 2593 ″ 3-aminophenylethyl 2594 ″ 3-methylsulfonylamino- phenylethyl 2595 ″ 3-trifluoromethyl- sulfonylamino-phenylethyl 2596 ″ 3-hydroxymethylene- phenylethyl 2597 ″ 3-aminomethylene- phenylethyl 2598 ″ 3-tetrazolephenylethyl 2599 ″ 3-tertbutylamino- sulfonylphenylethyl 2600 ″ 3-aminosulfonyl-phenylethyl 2601 ″ 3-methoxyphenylethyl 2602 ″ 4-phenylphenylmethyl 2603 ″ 4-(2- hydroxymethylenephenyl)- phenylmethyl 2604 ″ 4-(2-tert-butyl- aminosufonyl-phenyl)- phenylmethyl 2605 ″ 4-(2-methylamino- sufonylphenyl)-phenylmethyl 2606 ″ 4-(2-ethylamino- sufonylphenyl)-phenylmethyl 2607 ″ 4-(2-aminosufonylphenyl)- phenylmethyl 2608 ″ 4-(2-chlorophenyl)- phenylmethyl 2609 ″ 4-(2-fluorophenyl)- phenylmethyl 2610 ″ 4-(2,4-dichlorophenyl)- phenylmethyl 2611 ″ 4-(2,6-dichlorophenyl)- phenylmethyl 2612 ″ 4-(3,5-dichlorophenyl)- phenylmethyl 2613 ″ 4-(2,3-dichlorophenyl)- phenylmethyl 2614 ″ 4-(2-methylphenyl)- phenylmethyl 2615 ″ 4-(2-tetrazole-phenyl)- phenylmethyl 2616 ″ 4-(2-methoxy-phenyl)- phenylmethyl 2617 ″ 4-(2-tmethyl-phenyl)- phenylmethyl 2618 ″ 4-(2-formyl-phenyl)- phenylmethyl 2619 ″ 4-(2-amino-phenyl)- phenylmethyl 2620 ″ 4-(2-methylamino-phenyl)- phenylmethyl 2621 ″ 4-(2-ethylamino-phenyl)- phenylmethyl 2622 ″ 4-(2-propylamino-phenyl)- phenylmethyl 2623 ″ 4-(2-methylsulfonylamino- phenyl)-phenylmethyl 2624 ″ 4-(2- trifluoromethylsulfonyl- amino-phenyl)-phenylmethyl 2625 ″ 4-(3-methylphenyl)- phenylmethyl 2626 ″ 4-(3-isopropylphenyl)- phenylmethyl 2627 ″ 4-(3- trifluoromethylsulfonyl- amino-phenyl)-phenylmethyl 2628 ″ 4-(3-methylsulfonylamino- phenyl)-phenylmethyl 2629 ″ 4-(3-amino-phenyl)- phenylmethyl 2630 ″ 4-(3-nitro-phenyl)- phenylmethyl 2631 2632 CH₃ H 2633 ″ methyl 2634 ″ ethyl 2635 ″ n-propyl 2636 ″ n-butyl 2637 ″ n-pentyl 2638 ″ n-hexanyl 2639 ″ n-heptanyl 2640 ″ isopropyl 2641 ″ tert-butyl 2642 ″ cyclopropyl 2643 ″ cyclobutanyl 2644 ″ cyclpentanyl 2645 ″ cyclohexanyl 2646 ″ cycloheptanyl 2647 ″ phenyl 2648 ″ phenylmethyl 2649 ″ 3-hydroxyphenyl 2650 ″ 3-hydroxy-4-methoxyphenyl 2651 ″ 3-fluorophenyl 2652 ″ 3-chlorophenyl 2653 ″ 3-nitrophenyl 2654 ″ 3-aminophenyl 2655 ″ 3-methyl-sulfonamidephenyl 2656 ″ 3-trifluoro- methylsulfonamidephenyl 2657 ″ 3-Ac—NHphenyl 2658 ″ 3-Boc—NHphenyl 2659 ″ 3-Cbz—NHphenyl 2660 ″ 3-aminomethylenephenyl 2661 ″ 3-aminoethylenephenyl 2662 ″ 3-cyanophenyl 2663 ″ 3-cyanomethylphenyl 2664 ″ 3-hydroxy-methylenephenyl 2665 ″ 3-carboxylphenyl 2666 ″ 3-mercaptophenyl 2667 ″ 3-methoxyphenyl 2668 ″ 3,4-methylene-dioxophenyl 2669 ″ 3-tetrazolephenyl 2670 ″ 3-aminosulfonylphenyl 2671 ″ 3-methylamino- sulfonylphenyl 2672 ″ 3-ethylamino-sulfonylphenyl 2673 ″ 3-tertbutylamino- sulfonylphenyl 2674 ″ 3-methylsulfonylphenyl 2675 ″ 4-methoxyphenyl 2676 ″ 4-phenylphenyl 2677 ″ 4-(2-hydroxymethylene- phenyl)-phenyl 2678 ″ 4-(2-tert-butylamino- sufonylphenyl)-phenyl 2679 ″ 4-(2-methylamino- sufonylphenyl)-phenyl 2680 ″ 4-(2-ethylamino- sufonylphenyl)-phenyl 2681 ″ 4-(2-aminosufonyl-phenyl)- phenyl 2682 ″ 4-(2-chlorophenyl)-phenyl 2683 ″ 4-(2-fluorophenyl)-phenyl 2684 ″ 4-(2,4-dichlorophenyl)- phenyl 2685 ″ 4-(2,6-dichlorophenyl)- phenyl 2686 ″ 4-(3,5-dichlorophenyl)- phenyl 2687 ″ 4-(2,3-dichlorophenyl)- phenyl 2688 ″ 4-(2-methylphenyl)-phenyl 2689 ″ 4-(2-tetrazole-phenyl)- phenyl 2690 ″ 4-(2-methoxy-phenyl)-phenyl 2691 ″ 4-(2-tmethyl-phenyl)-phenyl 2692 ″ 4-(2-formyl-phenyl)-phenyl 2693 ″ 4-(2-amino-phenyl)-phenyl 2694 ″ 4-(2-methylamino-phenyl)- phenyl 2695 ″ 4-(2-ethylamino-phenyl)- phenyl 2696 ″ 4-(2-propylamino-phenyl)- phenyl 2697 ″ 4-(2-methylsulfonylamino- phenyl)-phenyl 2698 ″ 4-(2- trifluoromethylsulfonyl- amino-phenyl)-phenyl 2699 ″ 4-(3-methylphenyl)-phenyl 2700 ″ 4-(3-isopropylphenyl)- phenyl 2701 ″ 4-(3- trifluoromethylsulfonyl- amino-phenyl)-phenyl 2702 ″ 4-(3-methylsulfonyl-amino- phenyl)-phenyl 2703 ″ 4-(3-amino-phenyl)-phenyl 2704 ″ 4-(3-nitro-phenyl)-phenyl 2705 ″ 2-pyridyl 2706 ″ 3-pyridyl 2707 ″ 4-pyridyl 2708 ″ 3-amino-4-pyridyl 2709 ″ 3-hydroxy-4-pyridyl 2710 ″ 3-imidazole 2711 ″ 2-nitro-3-imidazole 2712 ″ 5-thiazole 2713 ″ 5-oxazole 2714 ″ 4-pyazole 2715 ″ phenylethyl 2716 ″ 2-aminophenylethyl 2717 ″ 2-methylsulfonylamino- phenylethyl 2718 ″ 2- trifluoromethylsulfonylamino- phenylethyl 2719 ″ 2-hydroxymethylene- phenylethyl 2720 ″ 2-aminomethylene- phenylethyl 2721 ″ 2-tetrazolephenylethyl 2722 ″ 2-tertbutylamino- sulfonylphenylethyl 2723 ″ 2-aminosulfonyl-phenylethyl 2724 ″ 2-methoxyphenylethyl 2725 ″ 3-aminophenylethyl 2726 ″ 3-methylsulfonylamino- phenylethyl 2727 ″ 3-trifluoromethyl- sulfonylamino-phenylethyl 2728 ″ 3-hydroxy- methylenephenylethyl 2729 ″ 3-aminomethylene- phenylethyl 2730 ″ 3-tetrazolephenylethyl 2731 ″ 3-tertbutylamino- sulfonylphenylethyl 2732 ″ 3-aminosulfonyl-phenylethyl 2733 ″ 3-methoxyphenylethyl 2734 ″ 4-phenylphenylmethyl 2735 ″ 4-(2-hydroxy- methylenephenyl)- phenylmethyl 2736 ″ 4-(2-tert- butylaminosufonyl-phenyl)- phenylmethyl 2737 ″ 4-(2-methylamino- sufonylphenyl)-phenylmethyl 2738 ″ 4-(2-ethylamino- sufonylphenyl)-phenylmethyl 2739 ″ 4-(2-aminosufonyl-phenyl)- phenylmethyl 2740 ″ 4-(2-chlorophenyl)- phenylmethyl 2741 ″ 4-(2-fluorophenyl)- phenylmethyl 2742 ″ 4-(2,4-dichlorophenyl)- phenylmethyl 2743 ″ 4-(2,6-dichlorophenyl)- phenylmethyl 2744 ″ 4-(3,5-dichlorophenyl)- phenylmethyl 2745 ″ 4-(2,3-dichlorophenyl)- phenylmethyl 2746 ″ 4-(2-methylphenyl)- phenylmethyl 2747 ″ 4-(2-tetrazole-phenyl)- phenylmethyl 2748 ″ 4-(2-methoxy-phenyl)- phenylmethyl 2749 ″ 4-(2-tmethyl-phenyl)- phenylmethyl 2750 ″ 4-(2-formyl-phenyl)- phenylmethyl 2751 ″ 4-(2-amino-phenyl)- phenylmethyl 2752 ″ 4-(2-methylamino-phenyl)- phenylmethyl 2753 ″ 4-(2-ethylamino-phenyl)- phenylmethyl 2754 ″ 4-(2-propylamino-phenyl)- phenylmethyl 2755 ″ 4-(2-methylsulfonylamino- phenyl)-phenylmethyl 2756 ″ 4-(2- trifluoromethylsulfonyl- amino-phenyl)-phenylmethyl 2757 ″ 4-(3-methylphenyl)- phenylmethyl 2758 ″ 4-(3-isopropylphenyl)- phenylmethyl 2759 ″ 4-(3- trifluoromethylsulfonyl- amino-phenyl)-phenylmethyl 2760 ″ 4-(3-methylsulfonyl-amino- phenyl)-phenylmethyl 2761 ″ 4-(3-amino-phenyl)- phenylmethyl 2762 ″ 4-(3-nitro-phenyl)- phenylmethyl 2763 2764 3-phenylpropyl H 2765 ″ methyl 2766 ″ ethyl 2767 ″ n-propyl 2768 ″ n-butyl 2769 ″ n-pentyl 2770 ″ n-hexanyl 2771 ″ n-heptanyl 2772 ″ isopropyl 2773 ″ tert-butyl 2774 ″ cyclopropyl 2775 ″ cyclobutanyl 2776 ″ cyclpentanyl 2777 ″ cyclohexanyl 2778 ″ cycloheptanyl 2779 ″ phenyl 2780 ″ phenylmethyl 2781 ″ 3-hydroxyphenyl 2782 ″ 3-hydroxy-4-methoxyphenyl 2783 ″ 3-fluorophenyl 2784 ″ 3-chlorophenyl 2785 ″ 3-nitrophenyl 2786 ″ 3-aminophenyl 2787 ″ 3-methyl-sulfonamidephenyl 2788 ″ 3-trifluoro- methylsulfonamidephenyl 2789 ″ 3-Ac—NHphenyl 2790 ″ 3-Boc—NHphenyl 2791 ″ 3-Cbz—NHphenyl 2792 ″ 3-aminomethylenephenyl 2793 ″ 3-aminoethylenephenyl 2794 ″ 3-cyanophenyl 2795 ″ 3-cyanomethylphenyl 2796 ″ 3-hydroxy-methylenephenyl 2797 ″ 3-carboxylphenyl 2798 ″ 3-mercaptophenyl 2799 ″ 3-methoxyphenyl 2800 ″ 3,4-methylene-dioxophenyl 2801 ″ 3-tetrazolephenyl 2802 ″ 3-aminosulfonylphenyl 2803 ″ 3-methylamino- sulfonylphenyl 2804 ″ 3-ethylamino-sulfonylphenyl 2805 ″ 3-tertbutylamino- sulfonylphenyl 2806 ″ 3-methylsulfonylphenyl 2807 ″ 4-methoxyphenyl 2808 ″ 4-phenylphenyl 2809 ″ 4-(2-hydroxy- methylenephenyl)-phenyl 2810 ″ 4-(2-tert-butylamino- sufonylphenyl)-phenyl 2811 ″ 4-(2-methylamino- sufonylphenyl)-phenyl 2812 ″ 4-(2-ethylamino- sufonylphenyl)-phenyl 2813 ″ 4-(2-aminosufonyl-phenyl)- phenyl 2814 ″ 4-(2-chlorophenyl)-phenyl 2815 ″ 4-(2-fluorophenyl)-phenyl 2816 ″ 4-(2,4-dichlorophenyl)- phenyl 2817 ″ 4-(2,6-dichlorophenyl)- phenyl 2818 ″ 4-(3,5-dichlorophenyl)- phenyl 2819 ″ 4-(2,3-dichlorophenyl)- phenyl 2820 ″ 4-(2-methylphenyl)-phenyl 2821 ″ 4-(2-tetrazole-phenyl)- phenyl 2822 ″ 4-(2-methoxy-phenyl)-phenyl 2823 ″ 4-(2-tmethyl-phenyl)-phenyl 2824 ″ 4-(2-formyl-phenyl)-phenyl 2825 ″ 4-(2-amino-phenyl)-phenyl 2826 ″ 4-(2-methylamino-phenyl)- phenyl 2827 ″ 4-(2-ethylamino-phenyl)- phenyl 2828 ″ 4-(2-propylamino-phenyl)- phenyl 2829 ″ 4-(2-methylsulfonyl-amino- phenyl)-phenyl 2830 ″ 4-(2- trifluoromethylsulfonyl- amino-phenyl)-phenyl 2831 ″ 4-(3-methylphenyl)-phenyl 2832 ″ 4-(3-isopropylphenyl)- phenyl 2833 ″ 4-(3- trifluoromethylsulfonyl- amino-phenyl)-phenyl 2834 ″ 4-(3-methylsulfonyl-amino- phenyl)-phenyl 2835 ″ 4-(3-amino-phenyl)-phenyl 2836 ″ 4-(3-nitro-phenyl)-phenyl 2837 ″ 2-pyridyl 2838 ″ 3-pyridyl 2839 ″ 4-pyridyl 2840 ″ 3-amino-4-pyridyl 2841 ″ 3-hydroxy-4-pyridyl 2842 ″ 3-imidazole 2843 ″ 2-nitro-3-imidazole 2844 ″ 5-thiazole 2845 ″ 5-oxazole 2846 ″ 4-pyazole 2847 ″ phenylethyl 2848 ″ 2-aminophenylethyl 2849 ″ 2-methylsulfonylamino- phenylethyl 2850 ″ 2- trifluoromethylsulfonylamino- phenylethyl 2851 ″ 2-hydroxymethylene- phenylethyl 2852 ″ 2-aminomethylene- phenylethyl 2853 ″ 2-tetrazolephenylethyl 2854 ″ 2-tert-butylamino- sulfonylphenylethyl 2855 ″ 2-aminosulfonyl-phenylethyl 2856 ″ 2-methoxyphenyl 2857 ″ 3-aminophenylethyl 2858 ″ 3-methylsulfonylamino- phenylethyl 2859 ″ 3- trifluoromethylsulfonylamino- phenylethyl 2860 ″ 3-hydroxymethylene- phenylethyl 2861 ″ 3-aminomethylene- phenylethyl 2862 ″ 3-tetrazolephenylethyl 2863 ″ 3-tertbutylamino- sulfonylphenylethyl 2864 ″ 3-aminosulfonyl-phenylethyl 2865 ″ 3-methoxyphenylethyl 2866 ″ 4-phenylphenylmethyl 2867 ″ 4-(2-hydroxymethylene- phenyl)-phenylmethyl 2868 ″ 4-(2-tert- butylaminosufonyl-phenyl)- phenylmethyl 2869 ″ 4-(2-methylaminosufonyl- phenyl)-phenylmethyl 2870 ″ 4-(2-ethylaminosufonyl- phenyl)-phenylmethyl 2871 ″ 4-(2-aminosufonylphenyl)- phenylmethyl 2872 ″ 4-(2-chlorophenyl)- phenylmethyl 2873 ″ 4-(2-fluorophenyl)- phenylmethyl 2874 ″ 4-(2,4-dichlorophenyl)- phenylmethyl 2875 ″ 4-(2,6-dichlorophenyl)- phenylmethyl 2876 ″ 4-(3,5-dichlorophenyl)- phenylmethyl 2877 ″ 4-(2,3-dichlorophenyl)- phenylmethyl 2878 ″ 4-(2-methylphenyl)- phenylmethyl 2879 ″ 4-(2-tetrazole-phenyl)- phenylmethyl 2880 ″ 4-(2-methoxy-phenyl)- phenylmethyl 2881 ″ 4-(2-tmethyl-phenyl)- phenylmethyl 2882 ″ 4-(2-formyl-phenyl)- phenylmethyl 2883 ″ 4-(2-amino-phenyl)- phenylmethyl 2884 ″ 4-(2-methylamino-phenyl)- phenylmethyl 2885 ″ 4-(2-ethylamino-phenyl)- phenylmethyl 2886 ″ 4-(2-propylamino-phenyl)- phenylmethyl 2887 ″ 4-(2-methylsulfonylamino- phenyl)-phenylmethyl 2888 ″ 4-(2- trifluoromethylsulfonyl- amino-phenyl)-phenylmethyl 2889 ″ 4-(3-methylphenyl)- phenylmethyl 2890 ″ 4-(3-isopropylphenyl)- phenylmethyl 2891 ″ 4-(3- trifluoromethylsulfonyl- amino-phenyl)-phenylmethyl 2892 ″ 4-(3-methylsulfonylamino- phenyl)-phenylmethyl 2893 ″ 4-(3-amino-phenyl)- phenylmethyl 2894 ″ 4-(3-nitro-phenyl)- phenylmethyl 

What is claimed:
 1. A compound of the formula II:

or a pharmaceutically acceptable salt form or a steroisomer thereof, wherein: R¹ is selected from: —CO₂H, —C(O)NHOH, —C(O)NHOR⁷, —SH, and —CH₂CO₂R⁷; R² is selected from the formula: U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a) wherein: U is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a); X is absent or selected from C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, and C₂₋₁₀ alkynylene; Y is absent or selected from O, NR^(a), S(O)_(p), and C(O); Z is absent or selected from a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b); U^(a) is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a); X^(a) is absent or selected from C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, and C₂₋₁₀ alkynylene; Y^(a) is absent or selected from O, NR^(a), S(O)_(p), and C(O); Z^(a) is selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c); R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl and benzyl; R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl and benzyl; alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S; R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), C₁, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃; R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S; R³ is selected from the formula: U¹—X¹—Y¹—Z¹—U^(1a)—X^(1a)—Y^(1a)—Z^(1a) wherein: U¹ is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a); X¹ is absent or selected from C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, and C₂₋₁₀ alkynylene; Y¹ is absent or selected from O, NR^(a), S(O)_(p), and C(O); Z¹ is absent or selected from a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and piperidinyl substituted with 0-5 R^(b); U^(1a) is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a); X^(1a) is absent or selected from C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, and C₂₋₁₀ alkynylene; Y^(1a) is absent or selected from O, NR^(a), S(O)_(p), and C(O); Z^(1a) is selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c); R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl and benzyl; R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl and benzyl; alternatively, R^(a) and R^(a′) taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S; R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃; R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S; R⁵ is selected from: U²—X²—Y²—Z²—U^(2a)—X^(2a)—Y^(2a)—Z^(2a) wherein: U² is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a); X² is absent or selected from C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, and C₂₋₁₀ alkynylene; Y² is absent or selected from O, NR^(a), S(O)_(p), and C(O); Z² is absent or selected from a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b); U^(2a) is absent or is selected from: O, NR^(a), C(O), C(O)O, OC(O), C(O)NR^(a), NR^(a)C(O), OC(O)O, OC(O)NR^(a), NR^(a)C(O)O, NR^(a)C(O)NR^(a), S(O)_(p), S(O)_(p)NR^(a), NR^(a)S(O)_(p), and NR^(a)SO₂NR^(a); X^(2a) is absent or selected from C₁₋₁₀ alkylene, C₂₋₁₀ alkenylene, and C₂₋₁₀ alkynylene; Y^(2a) is absent or selected from O, NR^(a), S(O)_(p), and C(O); Z^(2a) is selected from H, a C₃₋₁₃ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c); R^(a), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl and benzyl; R^(a′), at each occurrence, is independently selected from H, C₁₋₄ alkyl, phenyl and benzyl; alternatively, R^(a) and R^(a′)taken together with the nitrogen to which they are attached form a 5 or 6 membered ring containing from 0-1 additional heteroatoms selected from the group consisting of N, O, and S; R^(b), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, and CF₂CF₃; R^(c), at each occurrence, is independently selected from C₁₋₆ alkyl, OR^(a), Cl, F, Br, I, ═O, CN, NO₂, NR^(a)R^(a′), C(O)R^(a), C(O)OR^(a), C(O)NR^(a)R^(a′), NR^(a)S(O)₂R^(a′), S(O)₂NR^(a)R^(a′), S(O)_(p)R^(a), CF₃, CF₂CF₃, and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S; R⁷ is selected from: C₁-C₁₀ alkyl, alkylaryl, and E is CH₂ or CO.
 2. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of claim
 1. 3. A method of treating an inflammatory disease in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 1. 4. A method of treating a condition or disease mediated by MMPs and/or TNF and/or aggrecanase in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 1. 5. A method of treating a condition or disease wherein the disease or condition is referred to as rheumatoid arthritis, osteoarthritis, periodontitis, gingivitis, corneal ulceration, solid tumor growth and tumor invasion by secondary metastases, neovascular glaucoma, multiple sclerosis, or psoriasis in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 1. 6. A method of treating a condition or disease wherein the disease or condition is referred to as fever, cardiovascular effects, hemorrhage, coagulation, cachexia, anorexia, alcoholism, acute phase response, acute infection, shock, graft versus host reaction, autoimmune disease or HIV infection in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 1. 7. A compound of claim 1, wherein: R¹ is selected from: —C(O)NHOH.
 8. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of claim
 7. 9. A method of treating an inflammatory disease in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 7. 10. A method of treating a condition or disease mediated by MMPs and/or TNF and/or aggrecanase in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 7. 11. A method of treating a condition or disease wherein the disease or condition is referred to as rheumatoid arthritis, osteoarthritis, periodontitis, gingivitis, corneal ulceration, solid tumor growth and tumor invasion by secondary metastases, neovascular glaucoma, multiple sclerosis, or psoriasis in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 7. 12. A method of treating a condition or disease wherein the disease or condition is referred to as fever, cardiovascular effects, hemorrhage, coagulation, cachexia, anorexia, alcoholism, acute phase response, acute infection, shock, graft versus host reaction, autoimmune disease or HIV infection in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 7. 13. A compound of claim 7, wherein: R¹ is —C(O)NHOH; R² is selected from the formula: U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a) wherein: U is absent or is selected from: O, NR^(a), C(O), C(O)O, C(O)NR^(a), NR^(a)C(O), S(O)_(p), S(O)_(p)NR^(a), and NR^(a)S(O)_(p); X is absent or selected from C₁₋₄ alkylene, C₂₋₄ alkenylene, and C₂₋₄ alkynylene; Y is absent or selected from O, NR^(a), S(O)_(p), and C(O); Z is absent or selected from a C₃₋₁₀ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b); U^(a) is absent or is selected from: O, NR^(a), C(O), C(O)O, C(O)NR^(a), NR^(a)C(O), S(O)_(p), S(O)_(p)NR^(a), and NR^(a)S(O)_(p); X^(a) is absent or selected from C₁₋₄ alkylene, C₂₋₄ alkenylene, and C₂₋₄ alkynylene; Y^(a) is absent or selected from O, NR^(a), S(O)_(p), and C(O); Z^(a) is selected from H, a C₃₋₁₀ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c); R³ is selected from the formula: U¹—X¹—Y¹—Z¹—U^(1a)—X^(1a)—Y^(1a)—Z^(1a) wherein: U¹ is absent or is selected from: O, NR^(a), C(O), C(O)O, C(O)NR^(a), NR^(a)C(O), S(O)_(p), S(O)_(p)NR^(a), and NR^(a)S(O)_(p); X¹ is absent or selected from C₁₋₄ alkylene, C₂₋₄ alkenylene, and C₂₋₄ alkynylene; Y¹ is absent or selected from O, NR^(a), S(O)_(p), and C(O); Z¹ is phenyl substituted with 0-5 R^(b); U^(1a) is absent or is selected from: O, NR^(a), C(O), C(O)O, C(O)NR^(a), NR^(a)C(O), S(O)_(p), S(O)_(p)NR^(a), and NR^(a)S(O)_(p); X^(1a) is absent or selected from C₁₋₄ alkylene, C₂₋₄ alkenylene, and C₂₋₄ alkynylene; Y^(1a) is absent or selected from O, NR^(a), S(O)_(p), and C(O); Z^(1a) is selected from H, a C₃₋₁₀ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c); R⁵ is selected from: U²—X²—Y²—Z²—U^(2a)—X^(2a)—Y^(2a)—Z^(2a) wherein: U² is absent or is selected from: O, NR^(a), C(O), C(O)O, C(O)NR^(a), NR^(a)C(O), S(O)_(p), S(O)_(p)NR^(a), and NR^(a)S(O)_(p); X² is absent or selected from C₁₋₄ alkylene, C₂₋₄ alkenylene, and C₂₋₄ alkynylene; Y² is absent or selected from O, NR^(a), S(O)_(p), and C(O); Z² is absent or selected from a C₃₋₁₀ carbocyclic residue substituted with 0-5 R^(b) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(b); U^(2a) is absent or is selected from: O, NR^(a), C(O), C(O)O, C(O)NR^(a), NR^(a)C(O), S(O)_(p), S(O)_(p)NR^(a), and NR^(a)S(O)_(p); X^(2a) is absent or selected from C₁₋₄ alkylene, C₂₋₄ alkenylene, and C₂₋₄ alkynylene; Y^(2a) is absent or selected from O, NR^(a), S(O)_(p), and C(O); Z^(2a) is selected from H, a C₃₋₁₀ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c); E is CH₂.
 14. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of claim
 13. 15. A method of treating an inflammatory disease in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 13. 16. A method of treating a condition or disease mediated by MMPs and/or TNF and/or aggrecanase in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 13. 17. A method of treating a condition or disease wherein the disease or condition is referred to as rheumatoid arthritis, osteoarthritis, periodontitis, gingivitis, corneal ulceration, solid tumor growth and tumor invasion by secondary metastases, neovascular glaucoma, multiple sclerosis, or psoriasis in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 13. 18. A method of treating a condition or disease wherein the disease or condition is referred to as fever, cardiovascular effects, hemorrhage, coagulation, cachexia, anorexia, alcoholism, acute phase response, acute infection, shock, graft versus host reaction, autoimmune disease or HIV infection in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 13. 19. A compound of claim 13 wherein: R⁵ is selected from: U²—X²—Y²—Z²—U^(2a)—X^(2a)—Y^(2a)—Z^(2a) wherein: U² is absent; X² is absent or is C₁₋₄ alkylene; Y² is absent; Z² is absent or phenyl substituted with 0-3 R^(b); U^(2a) is absent or is selected from: O and NR^(a); X^(2a) is absent or is C₁₋₄ alkylene; Y^(2a) is absent or selected from O and NR^(a); and Z^(2a) is selected from H, a C₃₋₁₀ carbocyclic residue substituted with 0-3 R^(c) and a 5-6 membered heterocyclic system containing from 1-2 heteroatoms selected from the group consisting of N, O, and S substituted with 0-3 R^(c).
 20. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of claim
 19. 21. A method of treating an inflammatory disease in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 19. 22. A method of treating a condition or disease mediated by MMPs and/or TNF and/or aggrecanase in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 19. 23. A method of treating a condition or disease wherein the disease or condition is referred to as rheumatoid arthritis, osteoarthritis, periodontitis, gingivitis, corneal ulceration, solid tumor growth and tumor invasion by secondary metastases, neovascular glaucoma, multiple sclerosis, or psoriasis in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 19. 24. A method of treating a condition or disease wherein the disease or condition is referred to as fever, cardiovascular effects, hemorrhage, coagulation, cachexia, anorexia, alcoholism, acute phase response, acute infection, shock, graft versus host reaction, autoimmune disease or HIV infection in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 19. 25. A compound of claim 19 wherein: R¹ is —C(O)NHOH; R² is selected from the formula: U—X—Y—Z—U^(a)—X^(a)—Y^(a)—Z^(a) wherein: U is absent or is selected from: NR^(a), C(O)NR^(a), NR^(a)C(O), S(O)_(p)NR^(a), and NR^(a)S(O)_(p); X is absent or is C₁₋₄ alkylene; Y is absent; Z is absent or selected from a C₃₋₇ cycloalkyl residue substituted with 0-3 R^(b), phenyl substituted with 0-3 R^(b), and a 5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-3 R^(b); U^(a) is absent or is selected from: O and NR^(a); X^(a) is absent or is C₁₋₄ alkylene; Y^(a) is absent or selected from O, NR^(a), S(O)_(p), and C(O); Z^(a) is selected from H, a C₃₋₇ cycloalkyl residue substituted with 0-3 R^(c), phenyl substituted with 0-3 R^(c), and a 5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-3 R^(c); R³ is selected from the formula: U¹—X¹—Y¹—Z¹—U^(1a)—X^(1a)—Y^(1a)—Z^(1a) wherein: U¹ is absent or is selected from: O, NR^(a), C(O), C(O)O, C(O)NR^(a), NR^(a)C(O), S(O)_(p), S(O)_(p)NR^(a), and NR^(a)S(O)_(p); X¹ is absent or selected from C₁₋₄ alkylene, C₂₋₄ alkenylene, and C₂₋₄ alkynylene; Y¹ is absent or selected from O, NR^(a), S(O)_(p), and C(O); Z¹ is phenyl substituted with 0-5 R^(b); U^(1a) is absent or is selected from: O, NR^(a), C(O), C(O)O, C(O)NR^(a), NR^(a)C(O), S(O)_(p), S(O)_(p)NR^(a), and NR^(a)S(O)_(p); X^(1a) is absent or selected from C₁₋₄ alkylene, C₂₋₄ alkenylene, and C₂₋₄ alkynylene; Y^(1a) is absent or selected from O, NR^(a), S(O)_(p), and C(O); Z^(1a)is selected from H, a C₅₋₁₀ carbocyclic residue substituted with 0-5 R^(c) and a 5-14 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-5 R^(c); R⁵ is selected from: U²—X²—Y²—Z²—U^(2a)—X^(2a)—Y^(2a)—Z^(2a) wherein: U² is absent; X² is absent or is C₁₋₄ alkylene; Y² is absent; Z² is absent or phenyl substituted with 0-3 R^(b); U^(2a) is absent or is selected from: O and NR^(a); X^(2a) is absent or is C₁₋₄ alkylene; Y^(2a) is absent or selected from O and NR^(a); and Z^(2a) is selected from H, a C₅₋₁₀ carbocyclic residue substituted with 0-3 R^(c) and a 5-6 membered heterocyclic system containing from 1-2 heteroatoms selected from the group consisting of N, O, and S substituted with 0-3 R^(c).
 26. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of claim
 25. 27. A method of treating an inflammatory disease in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 25. 28. A method of treating a condition or disease mediated by MMPs and/or TNF and/or aggrecanase in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 25. 29. A method of treating a condition or disease wherein the disease or condition is referred to as rheumatoid arthritis, osteoarthritis, periodontitis, gingivitis, corneal ulceration, solid tumor growth and tumor invasion by secondary metastases, neovascular glaucoma, multiple sclerosis, or psoriasis in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 25. 30. A method of treating a condition or disease wherein the disease or condition is referred to as fever, cardiovascular effects, hemorrhage, coagulation, cachexia, anorexia, alcoholism, acute phase response, acute infection, shock, graft versus host reaction, autoimmune disease or HIV infection in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 25. 31. A compound is selected from the group consisting of: N1-(2(R)-hydroxy-1(S)-indanyl)-N4-hydroxy-2(R)-isobutyl-butanediamide; N1-(2(R)-hydroxy-1(S)-indanyl)-N4-hydroxy-2(R)-isobutyl-3(S)-(5-hydroxycarbonyl)-pentanamide; N1-(2(R)-hydroxy-1(S)-indanyl)-N4-hydroxy-2(R)-isobutyl-3(S)-methyl-butanediamide; N1-(2(R)-hydroxy-1(S)-indanyl)-N4-hydroxy-2(R)-isobutyl-3(S)-propyl-butanediamide; N1-(2(R)-hydroxy-1(S)-indanyl)-N4-hydroxy-2(R)-hexyl-3(S)-propyl-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(4-hydroxy-phenyl)methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(4-methoxy-phenyl)methyl]butanediamide; N1-[1(S)-indanyl]-N4-hydroxy-2(R)-[(4-hydroxy-phenyl)methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[3-phenyl-propyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(benzyloxy)-phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[3-(benzyloxy)-phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(4-fluoro-phenyl)methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3,4-methylenedioxy-phenyl)methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-methoxy-phenyl)methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3-trifluoromethyl-phenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2-tert-butylaminosulfonyl-phenyl)phenyl]methyl]-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2-methoxy-phenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-phenylphenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-4-methoxy-phenyl)methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2-chloro-phenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(benzofuran-2-yl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2-methyl-phenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[(3,4-methylenedioxy-phenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-((tetrazol-2-yl-phenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[3-phenylphenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[(3-methyl-phenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(4-amino-phenyl)methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[((4-benzyloxy-carbonyl)amino)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2-hydroxymethylphenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3,4,5-trimethoxy-phenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2,4-di-methoxy-phenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3,5-di-chloro-phenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2-trifluoromethyl-phenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3-isopropyl-phenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(2,4-dichloro-phenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3-chloro-4-fluoro-phenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(p-toluenesulfonyl-amino)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1S)-indanyl]-N4-hydroxy-2(R)-phenylmethyl-3(S)-(tert-butyloxy-carbonyl-amino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3,4-methylenedioxyphenyl)phenyl]methyl]-3(S)-(tert-butyloxy-carbonyl-amino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3-methoxyphenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3-fluorophenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-fluoro-phenyl)methyl]-3(S)-(tert-butyloxy-carbonyl-amino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(tert-butyloxy-carbonyl-amino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3-nitrophenyl)phenyl]methyl]butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[[4-(3-(methylsulfonyl-amino)-phenyl)phenyl]methyl]-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(3-trimethylsilyl-propyl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2,2-dimethyl-propionamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(ethyloxy-carbonyl-amino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(iso-butyloxy-carbonyl-amino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(propionamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-methyl-cyclopropane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2,2-dimethylpropyl-amino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(methylsulfonyl-amino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-amino-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(4-(methylsulfonylamino)-phenyl)methyl]-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(cyclobutane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-hydroxymethyl-isobutanamide)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-hydroxyl-cyclopropane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-phenyl-cyclopropane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(bezene Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-cyano-cyclopropane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-phenyl-cyclopentane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-methyl-cyclohexane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-indole carboxamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-furan carboxamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-quinoline carboxamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(3,4,5-trimethoxy benzene Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-methyl-3-amino-benzene Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-methyl-6-amino-benzene Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(3-pyridine Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-(2,4-dichloro-phenyl)-cyclopropane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-(4-chloro-phenyl)-cyclopropane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(3-methylsulfonyl)-benzene Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-methylsulfonyl-benzene Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(3-cyano-benzene Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(6-quinoline carboxamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-ethyl,3-methyl-pyrazole 5-carboxamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3-(4-morpholino-benzene Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-chloro-4-methylsulfonyl-benzene Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(4-(imidazol-1-yl)benzene Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-thiophene Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-tert-butyl, 3-methyl-pyrazole 5-carboxamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(4-aminomethyl benzene Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-hydroxyl-isobutanamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(cyclopropane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(cyclopentane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-cyclopentyl acetamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(cyclohexane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(4-(4-N-Boc-piperazinyl-1-yl)benzene Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(4-(piperazinyl-1-yl)benzene Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-fluoro-6-chloro-benzene Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-amino-cyclohexane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-methylthio-acetamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-methoxy-acetamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-allyl-cyclopentane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-n-propyl-cyclopentane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-allyl-cyclopropane Carboxamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(8-quinoline-sulfonamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(4-nitro-benzene sulfonamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1,4-di-methyl-2-chloro-pyrazole-3-sulfonamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1,5-dimethyl-isoxazole 3-sulfonamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1-methyl-imidazole 3-sulfonamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(benzene sulfonamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(1,4-dimethyl pyrazole 3-sulfonamido)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-methylsulfonyl benzene sulfonamido-1-yl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(cyclohexylamino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(iso-propylamino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[4-(2-trifluoromethylphenyl)-phenylmethyl]-3(S)-(2,2-dimethylpropyl-amino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(cyclopentylamino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(cyclopropylmethyl)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(benzylamino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-furanylmethylamino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-4-methylphenyl)methyl]-3(S)-(3-cyanophenylmethylamino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2,2-dimethylpropyl-amino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-pentylamino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(bis-cyclopropylmethylamino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3(S)-(2-thiophenylmethylamino)-butanediamide; N1-[2(R)-hydroxy-1(S)-indanyl]-N4-hydroxy-2(R)-[(3-hydroxy-phenyl)methyl]-3()-(2-methyl-propylamino)-butanediamide; or a pharmaceutically acceptable salt form or a steroisomer thereof.
 32. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of claim
 31. 33. A method of treating an inflammatory disease in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 31. 34. A method of treating a condition or disease mediated by MMPs and/or TNF and/or aggrecanase in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 31. 35. A method of treating a condition or disease wherein the disease or condition is referred to as rheumatoid arthritis, osteoarthritis, periodontitis, gingivitis, corneal ulceration, solid tumor growth and tumor invasion by secondary metastases, neovascular glaucoma, multiple sclerosis, or psoriasis in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 31. 36. A method of treating a condition or disease wherein the disease or condition is referred to as fever, cardiovascular effects, hemorrhage, coagulation, cachexia, anorexia, alcoholism, acute phase response, acute infection, shock, graft versus host reaction, autoimmune disease or HIV infection in a mammal comprising administering to the mammal in need of such treatment a therapeutically effective amount of a compound of claim
 31. 